Canonical Allele Identifier: CA1602345253

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724651_174724654delinsAGAG , CM000667.2:g.174724651_174724654delinsAGAG	GRCh38
NC_000005.9:g.174151654_174151657delinsAGAG , CM000667.1:g.174151654_174151657delinsAGAG	GRCh37
NC_000005.8:g.174084260_174084263delinsAGAG	NCBI36
NG_008124.1:g.5080_5083delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.-9_-6delinsAGAG MANE Select	ENSP00000239243.5:n.-9_-6delinsAGAG
ENST00000239243.6:c.-9_-6delinsAGAG	ENSP00000239243.5:n.-9_-6delinsAGAG
ENST00000507785.2:c.-9_-6delinsAGAG	ENSP00000427425.1:n.-9_-6delinsAGAG
NM_002449.4:c.-9_-6delinsAGAG	NP_002440.2:n.-9_-6delinsAGAG
NM_001363626.1:c.-9_-6delinsAGAG	NP_001350555.1:n.-9_-6delinsAGAG
NM_002449.5:c.-9_-6delinsAGAG MANE Select	NP_002440.2:n.-9_-6delinsAGAG
NM_001363626.2:c.-9_-6delinsAGAG	NP_001350555.1:n.-9_-6delinsAGAG