Canonical Allele Identifier: CA371893292
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837149C>A , CM000670.2:g.117837149C>A GRCh38
NC_000008.10:g.118849388C>A , CM000670.1:g.118849388C>A GRCh37
NC_000008.9:g.118918569C>A NCBI36
NG_007455.2:g.279671G>T , LRG_493:g.279671G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.482G>T
ENST00000378204.7:c.1015G>T MANE Select ENSP00000367446.3:p.Gly339Cys
ENST00000436216.2:c.383G>T
ENST00000378204.6:c.1015G>T ENSP00000367446.2:p.Gly339Cys
ENST00000436216.1:c.383G>T
ENST00000437196.1:c.74-1598G>T ENSP00000407299.1:n.74-1598G>T
NM_000127.2:c.1015G>T , LRG_493t1:c.1015G>T NP_000118.2:p.Gly339Cys
NM_000127.3:c.1015G>T MANE Select NP_000118.2:p.Gly339Cys