Canonical Allele Identifier: CA356139082
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864802G>C (hg19) chr4:g.4863075G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863075G>C , CM000666.2:g.4863075G>C GRCh38
NC_000004.11:g.4864802G>C , CM000666.1:g.4864802G>C GRCh37
NC_000004.10:g.4915703G>C NCBI36
NG_008121.1:g.8411G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.844G>C MANE Select ENSP00000372170.4:p.Ala282Pro
ENST00000382723.4:c.844G>C ENSP00000372170.4:p.Ala282Pro
NM_002448.3:c.844G>C MANE Select NP_002439.2:p.Ala282Pro
Search 100 bp 5'
Search 100 bp 3'