Canonical Allele Identifier: CA357140291
Gene: ENAM HGNC NCBI

Linked Data

gnomAD v4: 4-70642687-G-A

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1261G>A MANE Select ENSP00000379383.4:p.Gly421Ser
ENST00000396073.3:c.1261G>A ENSP00000379383.3:p.Gly421Ser
ENST00000472903.5:n.99+4844G>A
NM_031889.2:c.1261G>A NP_114095.2:p.Gly421Ser
XM_006714056.2:c.1261G>A XP_006714119.1:p.Gly421Ser
XM_006714056.4:c.1261G>A XP_006714119.1:p.Gly421Ser
NM_001368133.1:c.607G>A NP_001355062.1:p.Gly203Ser
NM_031889.3:c.1261G>A MANE Select NP_114095.2:p.Gly421Ser