Canonical Allele Identifier: CA439943404
Gene: ENAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.71508412A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642695A>G , CM000666.2:g.70642695A>G GRCh38
NC_000004.11:g.71508412A>G , CM000666.1:g.71508412A>G GRCh37
NC_000004.10:g.71727276A>G NCBI36
NG_013024.1:g.18952A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1269A>G MANE Select ENSP00000379383.4:p.Lys423=
ENST00000396073.3:c.1269A>G ENSP00000379383.3:p.Lys423=
ENST00000472903.5:n.99+4852A>G
NM_031889.2:c.1269A>G NP_114095.2:p.Lys423=
XM_006714056.2:c.1269A>G XP_006714119.1:p.Lys423=
XM_006714056.4:c.1269A>G XP_006714119.1:p.Lys423=
NM_001368133.1:c.615A>G NP_001355062.1:p.Lys205=
NM_031889.3:c.1269A>G MANE Select NP_114095.2:p.Lys423=