Canonical Allele Identifier: CA1466836123
Gene: ENAM HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628934T= , CM000666.2:g.70628934T= GRCh38
NC_000004.11:g.71494651T= , CM000666.1:g.71494651T= GRCh37
NG_013024.1:g.5191T=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-91T= MANE Select ENSP00000379383.4:n.-91T=
ENST00000396073.3:c.-91T= ENSP00000379383.3:n.-91T=
NM_031889.2:c.-91T= NP_114095.2:n.-91T=
XM_006714056.2:c.-567T= XP_006714119.1:n.-567T=
XM_006714056.4:c.-567T= XP_006714119.1:n.-567T=
NM_031889.3:c.-91T= MANE Select NP_114095.2:n.-91T=
Search 100 bp 5'
Search 100 bp 3'