Canonical Allele Identifier: CA2769499388

Gene: MSX2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724591_174724592del , CM000667.2:g.174724591_174724592del	GRCh38
NC_000005.9:g.174151594_174151595del , CM000667.1:g.174151594_174151595del	GRCh37
NC_000005.8:g.174084200_174084201del	NCBI36
NG_008124.1:g.5020_5021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.-69_-68del MANE Select	ENSP00000239243.5:n.-69_-68del
ENST00000239243.6:c.-69_-68del	ENSP00000239243.5:n.-69_-68del
NM_002449.4:c.-69_-68del	NP_002440.2:n.-69_-68del
NM_001363626.1:c.-69_-68del	NP_001350555.1:n.-69_-68del
NM_002449.5:c.-69_-68del MANE Select	NP_002440.2:n.-69_-68del
NM_001363626.2:c.-69_-68del	NP_001350555.1:n.-69_-68del