Canonical Allele Identifier: CA549707236
Gene: MSX1 HGNC NCBI

Linked Data

dbSNP Id: rs33929633

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862680_4862686dup , CM000666.2:g.4862680_4862686dup GRCh38
NC_000004.11:g.4864407_4864413dup , CM000666.1:g.4864407_4864413dup GRCh37
NC_000004.10:g.4915308_4915314dup NCBI36
NG_008121.1:g.8016_8022dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-21_470-15dup MANE Select ENSP00000372170.4:n.470-21_470-15dup
ENST00000382723.4:c.470-21_470-15dup ENSP00000372170.4:n.470-21_470-15dup
ENST00000468421.1:n.182-21_182-15dup
NM_002448.3:c.470-21_470-15dup MANE Select NP_002439.2:n.470-21_470-15dup