Canonical Allele Identifier: CA357139845
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642590A>T , CM000666.2:g.70642590A>T GRCh38
NC_000004.11:g.71508307A>T , CM000666.1:g.71508307A>T GRCh37
NC_000004.10:g.71727171A>T NCBI36
NG_013024.1:g.18847A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1164A>T MANE Select ENSP00000379383.4:p.Arg388Ser
ENST00000396073.3:c.1164A>T ENSP00000379383.3:p.Arg388Ser
ENST00000472903.5:n.99+4747A>T
NM_031889.2:c.1164A>T NP_114095.2:p.Arg388Ser
XM_006714056.2:c.1164A>T XP_006714119.1:p.Arg388Ser
XM_006714056.4:c.1164A>T XP_006714119.1:p.Arg388Ser
NM_001368133.1:c.510A>T NP_001355062.1:p.Arg170Ser
NM_031889.3:c.1164A>T MANE Select NP_114095.2:p.Arg388Ser