Canonical Allele Identifier: CA1466851503
Gene: ENAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642712G= , CM000666.2:g.70642712G= GRCh38
NC_000004.11:g.71508429G= , CM000666.1:g.71508429G= GRCh37
NC_000004.10:g.71727293G= NCBI36
NG_013024.1:g.18969G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396073.4:c.1286G= MANE Select ENSP00000379383.4:p.Arg429=
ENST00000396073.3:c.1286G= ENSP00000379383.3:p.Arg429=
ENST00000472903.5:n.99+4869G=
NM_031889.2:c.1286G= NP_114095.2:p.Arg429=
XM_006714056.2:c.1286G= XP_006714119.1:p.Arg429=
XM_006714056.4:c.1286G= XP_006714119.1:p.Arg429=
NM_001368133.1:c.632G= NP_001355062.1:p.Arg211=
NM_031889.3:c.1286G= MANE Select NP_114095.2:p.Arg429=