Canonical Allele Identifier: CA1435013839
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs1737963680

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4863168_4863169insT , CM000666.2:g.4863168_4863169insT GRCh38
NC_000004.11:g.4864895_4864896insT , CM000666.1:g.4864895_4864896insT GRCh37
NC_000004.10:g.4915796_4915797insT NCBI36
NG_008121.1:g.8504_8505insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.*25_*26insT MANE Select ENSP00000372170.4:n.*25_*26insT
ENST00000382723.4:c.*25_*26insT ENSP00000372170.4:n.*25_*26insT
NM_002448.3:c.*25_*26insT MANE Select NP_002439.2:n.*25_*26insT