Canonical Allele Identifier: CA1813949899
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117819807G= , CM000670.2:g.117819807G= GRCh38
NC_000008.10:g.118832046G= , CM000670.1:g.118832046G= GRCh37
NC_000008.9:g.118901227G= NCBI36
NG_007455.2:g.297013C= , LRG_493:g.297013C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.885-13C=
ENST00000378204.7:c.1418-13C= MANE Select ENSP00000367446.3:n.1418-13C=
ENST00000378204.6:c.1418-13C= ENSP00000367446.2:n.1418-13C=
ENST00000437196.1:c.*309-13C= ENSP00000407299.1:n.*309-13C=
NM_000127.2:c.1418-13C= , LRG_493t1:c.1418-13C= NP_000118.2:n.1418-13C=
NM_000127.3:c.1418-13C= MANE Select NP_000118.2:n.1418-13C=