Canonical Allele Identifier: CA1435013909

Gene: MSX1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4863273_4863275delinsCTT , CM000666.2:g.4863273_4863275delinsCTT	GRCh38
NC_000004.11:g.4865000_4865002delinsCTT , CM000666.1:g.4865000_4865002delinsCTT	GRCh37
NC_000004.10:g.4915901_4915903delinsCTT	NCBI36
NG_008121.1:g.8609_8611delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.*130_*132delinsCTT MANE Select	ENSP00000372170.4:n.*130_*132delinsCTT
ENST00000382723.4:c.*130_*132delinsCTT	ENSP00000372170.4:n.*130_*132delinsCTT
NM_002448.3:c.*130_*132delinsCTT MANE Select	NP_002439.2:n.*130_*132delinsCTT