Canonical Allele Identifier: CA2669788566
Gene: MSX1 HGNC NCBI

Linked Data

gnomAD v4: 4-4862710-G-GC

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862716dup , CM000666.2:g.4862716dup GRCh38
NC_000004.11:g.4864443dup , CM000666.1:g.4864443dup GRCh37
NC_000004.10:g.4915344dup NCBI36
NG_008121.1:g.8052dup

Transcript Alleles

HGVS Amino-acid change
ENST00000382723.5:c.485dup MANE Select ENSP00000372170.4:p.Ala163SerfsTer12
ENST00000382723.4:c.485dup ENSP00000372170.4:p.Ala163SerfsTer12
ENST00000468421.1:n.197dup
NM_002448.3:c.485dup MANE Select NP_002439.2:p.Ala163SerfsTer12