Canonical Allele Identifier: CA2669788704

Gene: MSX1

Linked Data

• gnomAD v4: 4-4863271-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.4863271_4863272insA , CM000666.2:g.4863271_4863272insA	GRCh38
NC_000004.11:g.4864998_4864999insA , CM000666.1:g.4864998_4864999insA	GRCh37
NC_000004.10:g.4915899_4915900insA	NCBI36
NG_008121.1:g.8607_8608insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382723.5:c.*128_*129insA MANE Select	ENSP00000372170.4:n.*128_*129insA
ENST00000382723.4:c.*128_*129insA	ENSP00000372170.4:n.*128_*129insA
NM_002448.3:c.*128_*129insA MANE Select	NP_002439.2:n.*128_*129insA