Canonical Allele Identifier: CA357139849
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642591G>T , CM000666.2:g.70642591G>T GRCh38
NC_000004.11:g.71508308G>T , CM000666.1:g.71508308G>T GRCh37
NC_000004.10:g.71727172G>T NCBI36
NG_013024.1:g.18848G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1165G>T MANE Select ENSP00000379383.4:p.Gly389Cys
ENST00000396073.3:c.1165G>T ENSP00000379383.3:p.Gly389Cys
ENST00000472903.5:n.99+4748G>T
NM_031889.2:c.1165G>T NP_114095.2:p.Gly389Cys
XM_006714056.2:c.1165G>T XP_006714119.1:p.Gly389Cys
XM_006714056.4:c.1165G>T XP_006714119.1:p.Gly389Cys
NM_001368133.1:c.511G>T NP_001355062.1:p.Gly171Cys
NM_031889.3:c.1165G>T MANE Select NP_114095.2:p.Gly389Cys