Canonical Allele Identifier: CA357140312
Gene: ENAM HGNC NCBI

Linked Data

gnomAD v4: 4-70642691-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642691C>A , CM000666.2:g.70642691C>A GRCh38
NC_000004.11:g.71508408C>A , CM000666.1:g.71508408C>A GRCh37
NC_000004.10:g.71727272C>A NCBI36
NG_013024.1:g.18948C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1265C>A MANE Select ENSP00000379383.4:p.Pro422His
ENST00000396073.3:c.1265C>A ENSP00000379383.3:p.Pro422His
ENST00000472903.5:n.99+4848C>A
NM_031889.2:c.1265C>A NP_114095.2:p.Pro422His
XM_006714056.2:c.1265C>A XP_006714119.1:p.Pro422His
XM_006714056.4:c.1265C>A XP_006714119.1:p.Pro422His
NM_001368133.1:c.611C>A NP_001355062.1:p.Pro204His
NM_031889.3:c.1265C>A MANE Select NP_114095.2:p.Pro422His