Canonical Allele Identifier: CA1466836170
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs1738242609
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628957G>A , CM000666.2:g.70628957G>A GRCh38
NC_000004.11:g.71494674G>A , CM000666.1:g.71494674G>A GRCh37
NG_013024.1:g.5214G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-68G>A MANE Select ENSP00000379383.4:n.-68G>A
ENST00000396073.3:c.-68G>A ENSP00000379383.3:n.-68G>A
NM_031889.2:c.-68G>A NP_114095.2:n.-68G>A
XM_006714056.2:c.-544G>A XP_006714119.1:n.-544G>A
XM_006714056.4:c.-544G>A XP_006714119.1:n.-544G>A
NM_031889.3:c.-68G>A MANE Select NP_114095.2:n.-68G>A
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