Canonical Allele Identifier: CA1466836006
Gene: ENAM HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628851C= , CM000666.2:g.70628851C= GRCh38
NC_000004.11:g.71494568C= , CM000666.1:g.71494568C= GRCh37
NG_013024.1:g.5108C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-174C= MANE Select ENSP00000379383.4:n.-174C=
ENST00000396073.3:c.-174C= ENSP00000379383.3:n.-174C=
NM_031889.2:c.-174C= NP_114095.2:n.-174C=
XM_006714056.4:c.-650C= XP_006714119.1:n.-650C=
NM_031889.3:c.-174C= MANE Select NP_114095.2:n.-174C=
Search 100 bp 5'
Search 100 bp 3'