Canonical Allele Identifier: CA387651047

Gene: CDX2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27963294G>C , CM000675.2:g.27963294G>C	GRCh38
NC_000013.10:g.28537431G>C , CM000675.1:g.28537431G>C	GRCh37
NC_000013.9:g.27435431G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001265.6:c.763C>G MANE Select	NP_001256.4:p.Gln255Glu
ENST00000381020.8:c.763C>G MANE Select	ENSP00000370408.6:p.Gln255Glu
NM_001265.4:c.763C>G	NP_001256.3:p.Gln255Glu
NM_001265.5:c.763C>G	NP_001256.3:p.Gln255Glu
NM_001354700.1:c.759C>G	NP_001341629.1:p.Ser253Arg
NM_001354700.2:c.759C>G	NP_001341629.1:p.Ser253Arg
ENST00000381020.7:c.763C>G	ENSP00000370408.6:p.Gln255Glu
ENST00000548877.1:n.291C>G
XM_011534875.1:c.787C>G	XP_011533177.1:p.Gln263Glu
XM_011534875.2:c.787C>G	XP_011533177.1:p.Gln263Glu
XM_011534876.1:c.783C>G	XP_011533178.1:p.Ser261Arg
XM_011534876.2:c.783C>G	XP_011533178.1:p.Ser261Arg
XM_011534877.1:c.759C>G	XP_011533179.1:p.Ser253Arg
XM_011534878.1:c.436C>G	XP_011533180.1:p.Gln146Glu
XM_011534878.2:c.436C>G	XP_011533180.1:p.Gln146Glu
XM_011534879.1:c.412C>G	XP_011533181.1:p.Gln138Glu
XM_011534879.2:c.412C>G	XP_011533181.1:p.Gln138Glu
XM_011534880.1:c.367C>G	XP_011533182.1:p.Gln123Glu