Canonical Allele Identifier: CA1466835971
Gene: ENAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628823A= , CM000666.2:g.70628823A= GRCh38
NC_000004.11:g.71494540A= , CM000666.1:g.71494540A= GRCh37
NG_013024.1:g.5080A=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-202A= MANE Select ENSP00000379383.4:n.-202A=
ENST00000396073.3:c.-202A= ENSP00000379383.3:n.-202A=
NM_031889.2:c.-202A= NP_114095.2:n.-202A=
XM_006714056.4:c.-678A= XP_006714119.1:n.-678A=
NM_031889.3:c.-202A= MANE Select NP_114095.2:n.-202A=