Canonical Allele Identifier: CA1466835983
Gene: ENAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628840C= , CM000666.2:g.70628840C= GRCh38
NC_000004.11:g.71494557C= , CM000666.1:g.71494557C= GRCh37
NG_013024.1:g.5097C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-185C= MANE Select ENSP00000379383.4:n.-185C=
ENST00000396073.3:c.-185C= ENSP00000379383.3:n.-185C=
NM_031889.2:c.-185C= NP_114095.2:n.-185C=
XM_006714056.4:c.-661C= XP_006714119.1:n.-661C=
NM_031889.3:c.-185C= MANE Select NP_114095.2:n.-185C=
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