Canonical Allele Identifier: CA357139892
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642599T>A , CM000666.2:g.70642599T>A GRCh38
NC_000004.11:g.71508316T>A , CM000666.1:g.71508316T>A GRCh37
NC_000004.10:g.71727180T>A NCBI36
NG_013024.1:g.18856T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1173T>A MANE Select ENSP00000379383.4:p.Tyr391Ter
ENST00000396073.3:c.1173T>A ENSP00000379383.3:p.Tyr391Ter
ENST00000472903.5:n.99+4756T>A
NM_031889.2:c.1173T>A NP_114095.2:p.Tyr391Ter
XM_006714056.2:c.1173T>A XP_006714119.1:p.Tyr391Ter
XM_006714056.4:c.1173T>A XP_006714119.1:p.Tyr391Ter
NM_001368133.1:c.519T>A NP_001355062.1:p.Tyr173Ter
NM_031889.3:c.1173T>A MANE Select NP_114095.2:p.Tyr391Ter