Canonical Allele Identifier: CA356139176
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4864830A>G (hg19) chr4:g.4863103A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863103A>G , CM000666.2:g.4863103A>G GRCh38
NC_000004.11:g.4864830A>G , CM000666.1:g.4864830A>G GRCh37
NC_000004.10:g.4915731A>G NCBI36
NG_008121.1:g.8439A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.872A>G MANE Select ENSP00000372170.4:p.Tyr291Cys
ENST00000382723.4:c.872A>G ENSP00000372170.4:p.Tyr291Cys
NM_002448.3:c.872A>G MANE Select NP_002439.2:p.Tyr291Cys
Search 100 bp 5'
Search 100 bp 3'