Canonical Allele Identifier: CA362229062

Gene: MSX2

Linked Data

• gnomAD v4: 5-174724732-G-T
• MyVariant Identifiers: chr5:g.174151735G>T (hg19) ; chr5:g.174724732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724732G>T , CM000667.2:g.174724732G>T	GRCh38
NC_000005.9:g.174151735G>T , CM000667.1:g.174151735G>T	GRCh37
NC_000005.8:g.174084341G>T	NCBI36
NG_008124.1:g.5161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.73G>T MANE Select	ENSP00000239243.5:p.Gly25Cys
ENST00000239243.6:c.73G>T	ENSP00000239243.5:p.Gly25Cys
ENST00000507785.2:c.73G>T	ENSP00000427425.1:p.Gly25Cys
NM_002449.4:c.73G>T	NP_002440.2:p.Gly25Cys
NM_001363626.1:c.73G>T	NP_001350555.1:p.Gly25Cys
NM_002449.5:c.73G>T MANE Select	NP_002440.2:p.Gly25Cys
NM_001363626.2:c.73G>T	NP_001350555.1:p.Gly25Cys