Canonical Allele Identifier: CA362228969
Gene: MSX2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174724687T>G , CM000667.2:g.174724687T>G GRCh38
NC_000005.9:g.174151690T>G , CM000667.1:g.174151690T>G GRCh37
NC_000005.8:g.174084296T>G NCBI36
NG_008124.1:g.5116T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000239243.7:c.28T>G MANE Select ENSP00000239243.5:p.Leu10Val
ENST00000239243.6:c.28T>G ENSP00000239243.5:p.Leu10Val
ENST00000507785.2:c.28T>G ENSP00000427425.1:p.Leu10Val
NM_002449.4:c.28T>G NP_002440.2:p.Leu10Val
NM_001363626.1:c.28T>G NP_001350555.1:p.Leu10Val
NM_002449.5:c.28T>G MANE Select NP_002440.2:p.Leu10Val
NM_001363626.2:c.28T>G NP_001350555.1:p.Leu10Val