Canonical Allele Identifier: CA447978543

Gene: MSX2

Linked Data

• MyVariant Identifiers: chr5:g.174151917C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724914C>G , CM000667.2:g.174724914C>G	GRCh38
NC_000005.9:g.174151917C>G , CM000667.1:g.174151917C>G	GRCh37
NC_000005.8:g.174084523C>G	NCBI36
NG_008124.1:g.5343C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000239243.7:c.255C>G MANE Select	ENSP00000239243.5:p.Gly85=
ENST00000239243.6:c.255C>G	ENSP00000239243.5:p.Gly85=
ENST00000507785.2:c.255C>G	ENSP00000427425.1:p.Gly85=
NM_002449.4:c.255C>G	NP_002440.2:p.Gly85=
NM_001363626.1:c.255C>G	NP_001350555.1:p.Gly85=
NM_002449.5:c.255C>G MANE Select	NP_002440.2:p.Gly85=
NM_001363626.2:c.255C>G	NP_001350555.1:p.Gly85=