Canonical Allele Identifier: CA371893290
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117837148C>G , CM000670.2:g.117837148C>G GRCh38
NC_000008.10:g.118849387C>G , CM000670.1:g.118849387C>G GRCh37
NC_000008.9:g.118918568C>G NCBI36
NG_007455.2:g.279672G>C , LRG_493:g.279672G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000684189.1:n.483G>C
ENST00000378204.7:c.1016G>C MANE Select ENSP00000367446.3:p.Gly339Ala
ENST00000436216.2:c.384G>C
ENST00000378204.6:c.1016G>C ENSP00000367446.2:p.Gly339Ala
ENST00000436216.1:c.384G>C
ENST00000437196.1:c.74-1597G>C ENSP00000407299.1:n.74-1597G>C
NM_000127.2:c.1016G>C , LRG_493t1:c.1016G>C NP_000118.2:p.Gly339Ala
NM_000127.3:c.1016G>C MANE Select NP_000118.2:p.Gly339Ala