Canonical Allele Identifier: CA2676572785

Gene: MSX2

Linked Data

• gnomAD v4: 5-174725096-G-GAC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174725096_174725097insAC , CM000667.2:g.174725096_174725097insAC	GRCh38
NC_000005.9:g.174152099_174152100insAC , CM000667.1:g.174152099_174152100insAC	GRCh37
NC_000005.8:g.174084705_174084706insAC	NCBI36
NG_008124.1:g.5525_5526insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.379+58_379+59insAC MANE Select	ENSP00000239243.5:n.379+58_379+59insAC
ENST00000239243.6:c.379+58_379+59insAC	ENSP00000239243.5:n.379+58_379+59insAC
ENST00000507785.2:c.*3+29_*3+30insAC	ENSP00000427425.1:n.*3+29_*3+30insAC
NM_002449.4:c.379+58_379+59insAC	NP_002440.2:n.379+58_379+59insAC
NM_001363626.1:c.*3+29_*3+30insAC	NP_001350555.1:n.*3+29_*3+30insAC
NM_002449.5:c.379+58_379+59insAC MANE Select	NP_002440.2:n.379+58_379+59insAC
NM_001363626.2:c.*3+29_*3+30insAC	NP_001350555.1:n.*3+29_*3+30insAC