Canonical Allele Identifier: CA1435013365

Gene: MSX1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4862295_4862299delinsTTCTG , CM000666.2:g.4862295_4862299delinsTTCTG	GRCh38
NC_000004.11:g.4864022_4864026delinsTTCTG , CM000666.1:g.4864022_4864026delinsTTCTG	GRCh37
NC_000004.10:g.4914923_4914927delinsTTCTG	NCBI36
NG_008121.1:g.7631_7635delinsTTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.470-406_470-402delinsTTCTG MANE Select	ENSP00000372170.4:n.470-406_470-402delinsTTCTG
ENST00000382723.4:c.470-406_470-402delinsTTCTG	ENSP00000372170.4:n.470-406_470-402delinsTTCTG
NM_002448.3:c.470-406_470-402delinsTTCTG MANE Select	NP_002439.2:n.470-406_470-402delinsTTCTG