Canonical Allele Identifier: CA357139826
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642586C>T , CM000666.2:g.70642586C>T GRCh38
NC_000004.11:g.71508303C>T , CM000666.1:g.71508303C>T GRCh37
NC_000004.10:g.71727167C>T NCBI36
NG_013024.1:g.18843C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1160C>T MANE Select ENSP00000379383.4:p.Ser387Leu
ENST00000396073.3:c.1160C>T ENSP00000379383.3:p.Ser387Leu
ENST00000472903.5:n.99+4743C>T
NM_031889.2:c.1160C>T NP_114095.2:p.Ser387Leu
XM_006714056.2:c.1160C>T XP_006714119.1:p.Ser387Leu
XM_006714056.4:c.1160C>T XP_006714119.1:p.Ser387Leu
NM_001368133.1:c.506C>T NP_001355062.1:p.Ser169Leu
NM_031889.3:c.1160C>T MANE Select NP_114095.2:p.Ser387Leu