Canonical Allele Identifier: CA1813957357
Gene: EXT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837090G= , CM000670.2:g.117837090G= GRCh38
NC_000008.10:g.118849329G= , CM000670.1:g.118849329G= GRCh37
NC_000008.9:g.118918510G= NCBI36
NG_007455.2:g.279730C= , LRG_493:g.279730C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.523+18C=
ENST00000378204.7:c.1056+18C= MANE Select ENSP00000367446.3:n.1056+18C=
ENST00000436216.2:c.424+18C=
ENST00000378204.6:c.1056+18C= ENSP00000367446.2:n.1056+18C=
ENST00000436216.1:c.424+18C=
ENST00000437196.1:c.74-1539C= ENSP00000407299.1:n.74-1539C=
NM_000127.2:c.1056+18C= , LRG_493t1:c.1056+18C= NP_000118.2:n.1056+18C=
NM_000127.3:c.1056+18C= MANE Select NP_000118.2:n.1056+18C=