Canonical Allele Identifier: CA438365412
Gene: MSX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.4862043G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4860316G>A , CM000666.2:g.4860316G>A GRCh38
NC_000004.11:g.4862043G>A , CM000666.1:g.4862043G>A GRCh37
NC_000004.10:g.4912944G>A NCBI36
NG_008121.1:g.5652G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.417G>A MANE Select ENSP00000372170.4:p.Lys139=
ENST00000382723.4:c.417G>A ENSP00000372170.4:p.Lys139=
NM_002448.3:c.417G>A MANE Select NP_002439.2:p.Lys139=
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