Canonical Allele Identifier: CA1466836158
Gene: ENAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628947G= , CM000666.2:g.70628947G= GRCh38
NC_000004.11:g.71494664G= , CM000666.1:g.71494664G= GRCh37
NG_013024.1:g.5204G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-78G= MANE Select ENSP00000379383.4:n.-78G=
ENST00000396073.3:c.-78G= ENSP00000379383.3:n.-78G=
NM_031889.2:c.-78G= NP_114095.2:n.-78G=
XM_006714056.2:c.-554G= XP_006714119.1:n.-554G=
XM_006714056.4:c.-554G= XP_006714119.1:n.-554G=
NM_031889.3:c.-78G= MANE Select NP_114095.2:n.-78G=