Canonical Allele Identifier: CA439943361
Gene: ENAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.71508403G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642686G>A , CM000666.2:g.70642686G>A GRCh38
NC_000004.11:g.71508403G>A , CM000666.1:g.71508403G>A GRCh37
NC_000004.10:g.71727267G>A NCBI36
NG_013024.1:g.18943G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1260G>A MANE Select ENSP00000379383.4:p.Leu420=
ENST00000396073.3:c.1260G>A ENSP00000379383.3:p.Leu420=
ENST00000472903.5:n.99+4843G>A
NM_031889.2:c.1260G>A NP_114095.2:p.Leu420=
XM_006714056.2:c.1260G>A XP_006714119.1:p.Leu420=
XM_006714056.4:c.1260G>A XP_006714119.1:p.Leu420=
NM_001368133.1:c.606G>A NP_001355062.1:p.Leu202=
NM_031889.3:c.1260G>A MANE Select NP_114095.2:p.Leu420=