Canonical Allele Identifier: CA2791245894
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44126941_44126942insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG , CM000673.2:g.44126941_44126942insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG GRCh38
NC_000011.9:g.44148491_44148492insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG , CM000673.1:g.44148491_44148492insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG GRCh37
NC_000011.8:g.44105067_44105068insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NCBI36
NG_007560.1:g.36393_36394insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG , LRG_494:g.36393_36394insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000342656.3:p.Leu356ThrfsTer19
ENST00000395673.8:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000379032.4:p.Leu356ThrfsTer19
ENST00000531161.6:n.1224_1225insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000682359.1:c.939+1957_939+1958insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000508226.1:n.939+1957_939+1958insACATGGACAAAGCAGGCAAAT...
ENST00000682711.1:c.-544+31089_-544+31090insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000506803.1:n.-544+31089_-544+31090insACATGGACAAAGCAGGC...
ENST00000682815.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000507234.1:p.Leu356ThrfsTer19
ENST00000682947.1:n.1239_1240insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000682993.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000507580.1:p.Leu356ThrfsTer19
ENST00000683000.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000508361.1:p.Leu356ThrfsTer19
ENST00000683299.1:n.1482_1483insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000683870.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000507922.1:p.Leu356ThrfsTer19
ENST00000683881.1:n.3626_3627insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000684039.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000507677.1:p.Leu356ThrfsTer19
ENST00000684124.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000508332.1:p.Leu356ThrfsTer19
ENST00000684533.1:c.744-3104_744-3103insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000507915.1:n.744-3104_744-3103insACATGGACAAAGCAGGCAAAT...
ENST00000533608.7:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG MANE Select ENSP00000431173.2:p.Leu356ThrfsTer19
ENST00000343631.3:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000342656.3:p.Leu356ThrfsTer19
ENST00000358681.8:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000351509.4:p.Leu356ThrfsTer19
ENST00000395673.7:c.1164_1165insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000379032.3:p.Leu389ThrfsTer19
ENST00000525559.1:n.39_40insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000531161.5:n.242_243insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG
ENST00000533608.5:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG ENSP00000431173.1:p.Leu356ThrfsTer19
NM_000401.3:c.1164_1165insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG , LRG_494t1:c.1164_1165insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_000392.3:p.Leu389ThrfsTer19
NM_001178083.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_001171554.1:p.Leu356ThrfsTer19
NM_207122.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG , LRG_494t2:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_997005.1:p.Leu356ThrfsTer19
XM_011519950.1:c.1203_1204insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG XP_011518252.1:p.Leu402ThrfsTer19
XM_011519951.1:c.1104_1105insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG XP_011518253.1:p.Leu369ThrfsTer19
XM_024448383.1:c.1203_1204insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG XP_024304151.1:p.Leu402ThrfsTer19
NM_001178083.2:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_001171554.1:p.Leu356ThrfsTer19
NM_207122.2:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG MANE Select NP_997005.1:p.Leu356ThrfsTer19
NM_001178083.3:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_001171554.1:p.Leu356ThrfsTer19
NM_001389628.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_001376557.1:p.Leu356ThrfsTer19
NM_001389630.1:c.1065_1066insACATGGACAAAGCAGGCAAATGTATCTTGCTTTTACCCCCATATTCATAAGG NP_001376559.1:p.Leu356ThrfsTer19