Canonical Allele Identifier: CA2762110800
Gene: ENAM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628962T>G , CM000666.2:g.70628962T>G GRCh38
NC_000004.11:g.71494679T>G , CM000666.1:g.71494679T>G GRCh37
NG_013024.1:g.5219T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-63T>G MANE Select ENSP00000379383.4:n.-63T>G
ENST00000396073.3:c.-63T>G ENSP00000379383.3:n.-63T>G
NM_031889.2:c.-63T>G NP_114095.2:n.-63T>G
XM_006714056.2:c.-539T>G XP_006714119.1:n.-539T>G
XM_006714056.4:c.-539T>G XP_006714119.1:n.-539T>G
NM_031889.3:c.-63T>G MANE Select NP_114095.2:n.-63T>G
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