Canonical Allele Identifier: CA371893306
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837155G>T , CM000670.2:g.117837155G>T GRCh38
NC_000008.10:g.118849394G>T , CM000670.1:g.118849394G>T GRCh37
NC_000008.9:g.118918575G>T NCBI36
NG_007455.2:g.279665C>A , LRG_493:g.279665C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.476C>A
ENST00000378204.7:c.1009C>A MANE Select ENSP00000367446.3:p.Pro337Thr
ENST00000436216.2:c.377C>A
ENST00000378204.6:c.1009C>A ENSP00000367446.2:p.Pro337Thr
ENST00000436216.1:c.377C>A
ENST00000437196.1:c.74-1604C>A ENSP00000407299.1:n.74-1604C>A
NM_000127.2:c.1009C>A , LRG_493t1:c.1009C>A NP_000118.2:p.Pro337Thr
NM_000127.3:c.1009C>A MANE Select NP_000118.2:p.Pro337Thr