Canonical Allele Identifier: CA362229668

Gene: MSX2

Linked Data

• MyVariant Identifiers: chr5:g.174152030C>G (hg19) ; chr5:g.174725027C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174725027C>G , CM000667.2:g.174725027C>G	GRCh38
NC_000005.9:g.174152030C>G , CM000667.1:g.174152030C>G	GRCh37
NC_000005.8:g.174084636C>G	NCBI36
NG_008124.1:g.5456C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.368C>G MANE Select	ENSP00000239243.5:p.Ser123Trp
ENST00000239243.6:c.368C>G	ENSP00000239243.5:p.Ser123Trp
ENST00000507785.2:c.368C>G	ENSP00000427425.1:p.Ser123Trp
NM_002449.4:c.368C>G	NP_002440.2:p.Ser123Trp
NM_001363626.1:c.368C>G	NP_001350555.1:p.Ser123Trp
NM_002449.5:c.368C>G MANE Select	NP_002440.2:p.Ser123Trp
NM_001363626.2:c.368C>G	NP_001350555.1:p.Ser123Trp