Canonical Allele Identifier: CA1063914651
Gene: ENAM HGNC NCBI

Linked Data

dbSNP Id: rs1738238963
gnomAD v3: 4-70628821-G-A
gnomAD v4: 4-70628821-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70628821G>A , CM000666.2:g.70628821G>A GRCh38
NC_000004.11:g.71494538G>A , CM000666.1:g.71494538G>A GRCh37
NG_013024.1:g.5078G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.-204G>A MANE Select ENSP00000379383.4:n.-204G>A
ENST00000396073.3:c.-204G>A ENSP00000379383.3:n.-204G>A
NM_031889.2:c.-204G>A NP_114095.2:n.-204G>A
XM_006714056.4:c.-680G>A XP_006714119.1:n.-680G>A
NM_031889.3:c.-204G>A MANE Select NP_114095.2:n.-204G>A
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