Canonical Allele Identifier: CA387651052

Gene: CDX2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27963296T>G , CM000675.2:g.27963296T>G	GRCh38
NC_000013.10:g.28537433T>G , CM000675.1:g.28537433T>G	GRCh37
NC_000013.9:g.27435433T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001265.6:c.761A>C MANE Select	NP_001256.4:p.Gln254Pro
ENST00000381020.8:c.761A>C MANE Select	ENSP00000370408.6:p.Gln254Pro
NM_001265.4:c.761A>C	NP_001256.3:p.Gln254Pro
NM_001265.5:c.761A>C	NP_001256.3:p.Gln254Pro
NM_001354700.1:c.757A>C	NP_001341629.1:p.Ser253Arg
NM_001354700.2:c.757A>C	NP_001341629.1:p.Ser253Arg
ENST00000381020.7:c.761A>C	ENSP00000370408.6:p.Gln254Pro
ENST00000548877.1:n.289A>C
XM_011534875.1:c.785A>C	XP_011533177.1:p.Gln262Pro
XM_011534875.2:c.785A>C	XP_011533177.1:p.Gln262Pro
XM_011534876.1:c.781A>C	XP_011533178.1:p.Ser261Arg
XM_011534876.2:c.781A>C	XP_011533178.1:p.Ser261Arg
XM_011534877.1:c.757A>C	XP_011533179.1:p.Ser253Arg
XM_011534878.1:c.434A>C	XP_011533180.1:p.Gln145Pro
XM_011534878.2:c.434A>C	XP_011533180.1:p.Gln145Pro
XM_011534879.1:c.410A>C	XP_011533181.1:p.Gln137Pro
XM_011534879.2:c.410A>C	XP_011533181.1:p.Gln137Pro
XM_011534880.1:c.365A>C	XP_011533182.1:p.Gln122Pro