Canonical Allele Identifier: CA357140410
Gene: ENAM HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.71508429G>C (hg19) chr4:g.70642712G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642712G>C , CM000666.2:g.70642712G>C GRCh38
NC_000004.11:g.71508429G>C , CM000666.1:g.71508429G>C GRCh37
NC_000004.10:g.71727293G>C NCBI36
NG_013024.1:g.18969G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000396073.4:c.1286G>C MANE Select ENSP00000379383.4:p.Arg429Pro
ENST00000396073.3:c.1286G>C ENSP00000379383.3:p.Arg429Pro
ENST00000472903.5:n.99+4869G>C
NM_031889.2:c.1286G>C NP_114095.2:p.Arg429Pro
XM_006714056.2:c.1286G>C XP_006714119.1:p.Arg429Pro
XM_006714056.4:c.1286G>C XP_006714119.1:p.Arg429Pro
NM_001368133.1:c.632G>C NP_001355062.1:p.Arg211Pro
NM_031889.3:c.1286G>C MANE Select NP_114095.2:p.Arg429Pro
Search 100 bp 5'
Search 100 bp 3'