Canonical Allele Identifier: CA357139859
Gene: ENAM HGNC NCBI

Linked Data

gnomAD v4: 4-70642592-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642592G>A , CM000666.2:g.70642592G>A GRCh38
NC_000004.11:g.71508309G>A , CM000666.1:g.71508309G>A GRCh37
NC_000004.10:g.71727173G>A NCBI36
NG_013024.1:g.18849G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1166G>A MANE Select ENSP00000379383.4:p.Gly389Asp
ENST00000396073.3:c.1166G>A ENSP00000379383.3:p.Gly389Asp
ENST00000472903.5:n.99+4749G>A
NM_031889.2:c.1166G>A NP_114095.2:p.Gly389Asp
XM_006714056.2:c.1166G>A XP_006714119.1:p.Gly389Asp
XM_006714056.4:c.1166G>A XP_006714119.1:p.Gly389Asp
NM_001368133.1:c.512G>A NP_001355062.1:p.Gly171Asp
NM_031889.3:c.1166G>A MANE Select NP_114095.2:p.Gly389Asp