Canonical Allele Identifier: CA1466835985
Gene: ENAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628842C= , CM000666.2:g.70628842C= GRCh38
NC_000004.11:g.71494559C= , CM000666.1:g.71494559C= GRCh37
NG_013024.1:g.5099C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396073.4:c.-183C= MANE Select ENSP00000379383.4:n.-183C=
ENST00000396073.3:c.-183C= ENSP00000379383.3:n.-183C=
NM_031889.2:c.-183C= NP_114095.2:n.-183C=
XM_006714056.4:c.-659C= XP_006714119.1:n.-659C=
NM_031889.3:c.-183C= MANE Select NP_114095.2:n.-183C=
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