Canonical Allele Identifier: CA439943481
Gene: ENAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.71508427T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642710T>C , CM000666.2:g.70642710T>C GRCh38
NC_000004.11:g.71508427T>C , CM000666.1:g.71508427T>C GRCh37
NC_000004.10:g.71727291T>C NCBI36
NG_013024.1:g.18967T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396073.4:c.1284T>C MANE Select ENSP00000379383.4:p.Val428=
ENST00000396073.3:c.1284T>C ENSP00000379383.3:p.Val428=
ENST00000472903.5:n.99+4867T>C
NM_031889.2:c.1284T>C NP_114095.2:p.Val428=
XM_006714056.2:c.1284T>C XP_006714119.1:p.Val428=
XM_006714056.4:c.1284T>C XP_006714119.1:p.Val428=
NM_001368133.1:c.630T>C NP_001355062.1:p.Val210=
NM_031889.3:c.1284T>C MANE Select NP_114095.2:p.Val428=