Canonical Allele Identifier: CA371892211
Gene: EXT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117835487C>G , CM000670.2:g.117835487C>G GRCh38
NC_000008.10:g.118847726C>G , CM000670.1:g.118847726C>G GRCh37
NC_000008.9:g.118916907C>G NCBI36
NG_007455.2:g.281333G>C , LRG_493:g.281333G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684189.1:n.588G>C
ENST00000378204.7:c.1121G>C MANE Select ENSP00000367446.3:p.Trp374Ser
ENST00000436216.2:c.489G>C
ENST00000378204.6:c.1121G>C ENSP00000367446.2:p.Trp374Ser
ENST00000436216.1:c.489G>C
ENST00000437196.1:c.*12G>C ENSP00000407299.1:n.*12G>C
NM_000127.2:c.1121G>C , LRG_493t1:c.1121G>C NP_000118.2:p.Trp374Ser
NM_000127.3:c.1121G>C MANE Select NP_000118.2:p.Trp374Ser