Canonical Allele Identifier: CA1602345386

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724709_174724710delinsGC , CM000667.2:g.174724709_174724710delinsGC	GRCh38
NC_000005.9:g.174151712_174151713delinsGC , CM000667.1:g.174151712_174151713delinsGC	GRCh37
NC_000005.8:g.174084318_174084319delinsGC	NCBI36
NG_008124.1:g.5138_5139delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.50_51delinsGC MANE Select	ENSP00000239243.5:p.Gly17=
ENST00000239243.6:c.50_51delinsGC	ENSP00000239243.5:p.Gly17=
ENST00000507785.2:c.50_51delinsGC	ENSP00000427425.1:p.Gly17=
NM_002449.4:c.50_51delinsGC	NP_002440.2:p.Gly17=
NM_001363626.1:c.50_51delinsGC	NP_001350555.1:p.Gly17=
NM_002449.5:c.50_51delinsGC MANE Select	NP_002440.2:p.Gly17=
NM_001363626.2:c.50_51delinsGC	NP_001350555.1:p.Gly17=