Canonical Allele Identifier: CA2760244921
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862686_4862687insTTTTTTTTTTTTTTTTCTT , CM000666.2:g.4862686_4862687insTTTTTTTTTTTTTTTTCTT GRCh38
NC_000004.11:g.4864413_4864414insTTTTTTTTTTTTTTTTCTT , CM000666.1:g.4864413_4864414insTTTTTTTTTTTTTTTTCTT GRCh37
NC_000004.10:g.4915314_4915315insTTTTTTTTTTTTTTTTCTT NCBI36
NG_008121.1:g.8022_8023insTTTTTTTTTTTTTTTTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT MANE Select ENSP00000372170.4:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT
ENST00000382723.4:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT ENSP00000372170.4:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT
ENST00000468421.1:n.182-15_182-14insTTTTTTTTTTTTTTTTCTT
NM_002448.3:c.470-15_470-14insTTTTTTTTTTTTTTTTCTT MANE Select NP_002439.2:n.470-15_470-14insTTTTTTTTTTTTTTTTCTT