Canonical Allele Identifier: CA357140293
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642687G>C , CM000666.2:g.70642687G>C GRCh38
NC_000004.11:g.71508404G>C , CM000666.1:g.71508404G>C GRCh37
NC_000004.10:g.71727268G>C NCBI36
NG_013024.1:g.18944G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1261G>C MANE Select ENSP00000379383.4:p.Gly421Arg
ENST00000396073.3:c.1261G>C ENSP00000379383.3:p.Gly421Arg
ENST00000472903.5:n.99+4844G>C
NM_031889.2:c.1261G>C NP_114095.2:p.Gly421Arg
XM_006714056.2:c.1261G>C XP_006714119.1:p.Gly421Arg
XM_006714056.4:c.1261G>C XP_006714119.1:p.Gly421Arg
NM_001368133.1:c.607G>C NP_001355062.1:p.Gly203Arg
NM_031889.3:c.1261G>C MANE Select NP_114095.2:p.Gly421Arg