Canonical Allele Identifier: CA1466836104
Gene: ENAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628914A= , CM000666.2:g.70628914A= GRCh38
NC_000004.11:g.71494631A= , CM000666.1:g.71494631A= GRCh37
NG_013024.1:g.5171A=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-111A= MANE Select ENSP00000379383.4:n.-111A=
ENST00000396073.3:c.-111A= ENSP00000379383.3:n.-111A=
NM_031889.2:c.-111A= NP_114095.2:n.-111A=
XM_006714056.2:c.-587A= XP_006714119.1:n.-587A=
XM_006714056.4:c.-587A= XP_006714119.1:n.-587A=
NM_031889.3:c.-111A= MANE Select NP_114095.2:n.-111A=
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