Canonical Allele Identifier: CA1466835997
Gene: ENAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628846G= , CM000666.2:g.70628846G= GRCh38
NC_000004.11:g.71494563G= , CM000666.1:g.71494563G= GRCh37
NG_013024.1:g.5103G=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-179G= MANE Select ENSP00000379383.4:n.-179G=
ENST00000396073.3:c.-179G= ENSP00000379383.3:n.-179G=
NM_031889.2:c.-179G= NP_114095.2:n.-179G=
XM_006714056.4:c.-655G= XP_006714119.1:n.-655G=
NM_031889.3:c.-179G= MANE Select NP_114095.2:n.-179G=
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