Canonical Allele Identifier: CA447978383

Gene: MSX2

Linked Data

• MyVariant Identifiers: chr5:g.174151803C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724800C>T , CM000667.2:g.174724800C>T	GRCh38
NC_000005.9:g.174151803C>T , CM000667.1:g.174151803C>T	GRCh37
NC_000005.8:g.174084409C>T	NCBI36
NG_008124.1:g.5229C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.141C>T MANE Select	ENSP00000239243.5:p.Phe47=
ENST00000239243.6:c.141C>T	ENSP00000239243.5:p.Phe47=
ENST00000507785.2:c.141C>T	ENSP00000427425.1:p.Phe47=
NM_002449.4:c.141C>T	NP_002440.2:p.Phe47=
NM_001363626.1:c.141C>T	NP_001350555.1:p.Phe47=
NM_002449.5:c.141C>T MANE Select	NP_002440.2:p.Phe47=
NM_001363626.2:c.141C>T	NP_001350555.1:p.Phe47=