Canonical Allele Identifier: CA357140346
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642699G>A , CM000666.2:g.70642699G>A GRCh38
NC_000004.11:g.71508416G>A , CM000666.1:g.71508416G>A GRCh37
NC_000004.10:g.71727280G>A NCBI36
NG_013024.1:g.18956G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1273G>A MANE Select ENSP00000379383.4:p.Gly425Ser
ENST00000396073.3:c.1273G>A ENSP00000379383.3:p.Gly425Ser
ENST00000472903.5:n.99+4856G>A
NM_031889.2:c.1273G>A NP_114095.2:p.Gly425Ser
XM_006714056.2:c.1273G>A XP_006714119.1:p.Gly425Ser
XM_006714056.4:c.1273G>A XP_006714119.1:p.Gly425Ser
NM_001368133.1:c.619G>A NP_001355062.1:p.Gly207Ser
NM_031889.3:c.1273G>A MANE Select NP_114095.2:p.Gly425Ser