Canonical Allele Identifier: CA447978424

Gene: MSX2

Linked Data

• MyVariant Identifiers: chr5:g.174151827C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724824C>T , CM000667.2:g.174724824C>T	GRCh38
NC_000005.9:g.174151827C>T , CM000667.1:g.174151827C>T	GRCh37
NC_000005.8:g.174084433C>T	NCBI36
NG_008124.1:g.5253C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.165C>T MANE Select	ENSP00000239243.5:p.Asp55=
ENST00000239243.6:c.165C>T	ENSP00000239243.5:p.Asp55=
ENST00000507785.2:c.165C>T	ENSP00000427425.1:p.Asp55=
NM_002449.4:c.165C>T	NP_002440.2:p.Asp55=
NM_001363626.1:c.165C>T	NP_001350555.1:p.Asp55=
NM_002449.5:c.165C>T MANE Select	NP_002440.2:p.Asp55=
NM_001363626.2:c.165C>T	NP_001350555.1:p.Asp55=