Canonical Allele Identifier: CA371893303
Gene: EXT1 HGNC NCBI

Linked Data

dbSNP Id: rs1812200901

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837154G>A , CM000670.2:g.117837154G>A GRCh38
NC_000008.10:g.118849393G>A , CM000670.1:g.118849393G>A GRCh37
NC_000008.9:g.118918574G>A NCBI36
NG_007455.2:g.279666C>T , LRG_493:g.279666C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.477C>T
ENST00000378204.7:c.1010C>T MANE Select ENSP00000367446.3:p.Pro337Leu
ENST00000436216.2:c.378C>T
ENST00000378204.6:c.1010C>T ENSP00000367446.2:p.Pro337Leu
ENST00000436216.1:c.378C>T
ENST00000437196.1:c.74-1603C>T ENSP00000407299.1:n.74-1603C>T
NM_000127.2:c.1010C>T , LRG_493t1:c.1010C>T NP_000118.2:p.Pro337Leu
NM_000127.3:c.1010C>T MANE Select NP_000118.2:p.Pro337Leu