Canonical Allele Identifier: CA1967883569
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44127030G= , CM000673.2:g.44127030G= GRCh38
NC_000011.9:g.44148580G= , CM000673.1:g.44148580G= GRCh37
NC_000011.8:g.44105156G= NCBI36
NG_007560.1:g.36482G= , LRG_494:g.36482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.1079+75G= ENSP00000342656.3:n.1079+75G=
ENST00000395673.8:c.1079+75G= ENSP00000379032.4:n.1079+75G=
ENST00000531161.6:n.1238+75G=
ENST00000682359.1:c.939+2046G= ENSP00000508226.1:n.939+2046G=
ENST00000682711.1:c.-544+31178G= ENSP00000506803.1:n.-544+31178G=
ENST00000682815.1:c.1079+75G= ENSP00000507234.1:n.1079+75G=
ENST00000682947.1:n.1253+75G=
ENST00000682993.1:c.1079+75G= ENSP00000507580.1:n.1079+75G=
ENST00000683000.1:c.1079+75G= ENSP00000508361.1:n.1079+75G=
ENST00000683299.1:n.1496+75G=
ENST00000683870.1:c.1079+75G= ENSP00000507922.1:n.1079+75G=
ENST00000683881.1:n.3640+75G=
ENST00000684039.1:c.1079+75G= ENSP00000507677.1:n.1079+75G=
ENST00000684124.1:c.1079+75G= ENSP00000508332.1:n.1079+75G=
ENST00000684533.1:c.744-3015G= ENSP00000507915.1:n.744-3015G=
ENST00000533608.7:c.1079+75G= MANE Select ENSP00000431173.2:n.1079+75G=
ENST00000343631.3:c.1079+75G= ENSP00000342656.3:n.1079+75G=
ENST00000358681.8:c.1079+75G= ENSP00000351509.4:n.1079+75G=
ENST00000395673.7:c.1178+75G= ENSP00000379032.3:n.1178+75G=
ENST00000525559.1:n.53+75G=
ENST00000531161.5:n.256+75G=
ENST00000533608.5:c.1079+75G= ENSP00000431173.1:n.1079+75G=
NM_000401.3:c.1178+75G= , LRG_494t1:c.1178+75G= NP_000392.3:n.1178+75G=
NM_001178083.1:c.1079+75G= NP_001171554.1:n.1079+75G=
NM_207122.1:c.1079+75G= , LRG_494t2:c.1079+75G= NP_997005.1:n.1079+75G=
XM_011519950.1:c.1217+75G= XP_011518252.1:n.1217+75G=
XM_011519951.1:c.1118+75G= XP_011518253.1:n.1118+75G=
XM_024448383.1:c.1217+75G= XP_024304151.1:n.1217+75G=
NM_001178083.2:c.1079+75G= NP_001171554.1:n.1079+75G=
NM_207122.2:c.1079+75G= MANE Select NP_997005.1:n.1079+75G=
NM_001178083.3:c.1079+75G= NP_001171554.1:n.1079+75G=
NM_001389628.1:c.1079+75G= NP_001376557.1:n.1079+75G=
NM_001389630.1:c.1079+75G= NP_001376559.1:n.1079+75G=