Canonical Allele Identifier: CA598980718

Gene: EXT2

Linked Data

• dbSNP Id: rs1389258099
• gnomAD v2: 11-44146554-TCTCGCAAAGG-T
• gnomAD v4: 11-44125004-TCTCGCAAAGG-T
• MyVariant Identifiers: chr11:g.44146555_44146564del (hg19) ; chr11:g.44125005_44125014del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44125008_44125017del , CM000673.2:g.44125008_44125017del	GRCh38
NC_000011.9:g.44146558_44146567del , CM000673.1:g.44146558_44146567del	GRCh37
NC_000011.8:g.44103134_44103143del	NCBI36
NG_007560.1:g.34460_34469del , LRG_494:g.34460_34469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.939+24_939+33del	ENSP00000342656.3:n.939+24_939+33del
ENST00000395673.8:c.939+24_939+33del	ENSP00000379032.4:n.939+24_939+33del
ENST00000531161.6:n.1098+24_1098+33del
ENST00000682359.1:c.939+24_939+33del	ENSP00000508226.1:n.939+24_939+33del
ENST00000682711.1:c.-544+29156_-544+29165del	ENSP00000506803.1:n.-544+29156_-544+29165del
ENST00000682815.1:c.939+24_939+33del	ENSP00000507234.1:n.939+24_939+33del
ENST00000682947.1:n.1113+24_1113+33del
ENST00000682993.1:c.939+24_939+33del	ENSP00000507580.1:n.939+24_939+33del
ENST00000683000.1:c.939+24_939+33del	ENSP00000508361.1:n.939+24_939+33del
ENST00000683299.1:n.1356+24_1356+33del
ENST00000683870.1:c.939+24_939+33del	ENSP00000507922.1:n.939+24_939+33del
ENST00000683881.1:n.3500+24_3500+33del
ENST00000684039.1:c.939+24_939+33del	ENSP00000507677.1:n.939+24_939+33del
ENST00000684124.1:c.939+24_939+33del	ENSP00000508332.1:n.939+24_939+33del
ENST00000684533.1:c.744-5037_744-5028del	ENSP00000507915.1:n.744-5037_744-5028del
ENST00000533608.7:c.939+24_939+33del MANE Select	ENSP00000431173.2:n.939+24_939+33del
ENST00000343631.3:c.939+24_939+33del	ENSP00000342656.3:n.939+24_939+33del
ENST00000358681.8:c.939+24_939+33del	ENSP00000351509.4:n.939+24_939+33del
ENST00000395673.7:c.1038+24_1038+33del	ENSP00000379032.3:n.1038+24_1038+33del
ENST00000531161.5:n.116+24_116+33del
ENST00000533608.5:c.939+24_939+33del	ENSP00000431173.1:n.939+24_939+33del
NM_000401.3:c.1038+24_1038+33del , LRG_494t1:c.1038+24_1038+33del	NP_000392.3:n.1038+24_1038+33del
NM_001178083.1:c.939+24_939+33del	NP_001171554.1:n.939+24_939+33del
NM_207122.1:c.939+24_939+33del , LRG_494t2:c.939+24_939+33del	NP_997005.1:n.939+24_939+33del
XM_011519950.1:c.1077+24_1077+33del	XP_011518252.1:n.1077+24_1077+33del
XM_011519951.1:c.978+24_978+33del	XP_011518253.1:n.978+24_978+33del
XM_024448383.1:c.1077+24_1077+33del	XP_024304151.1:n.1077+24_1077+33del
NM_001178083.2:c.939+24_939+33del	NP_001171554.1:n.939+24_939+33del
NM_207122.2:c.939+24_939+33del MANE Select	NP_997005.1:n.939+24_939+33del
NM_001178083.3:c.939+24_939+33del	NP_001171554.1:n.939+24_939+33del
NM_001389628.1:c.939+24_939+33del	NP_001376557.1:n.939+24_939+33del
NM_001389630.1:c.939+24_939+33del	NP_001376559.1:n.939+24_939+33del