Canonical Allele Identifier: CA1008513778
Gene: DDR2 HGNC NCBI

Linked Data

dbSNP Id: rs1659946065

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162691152T>C , CM000663.2:g.162691152T>C GRCh38
NC_000001.10:g.162660942T>C , CM000663.1:g.162660942T>C GRCh37
NC_000001.9:g.160927566T>C NCBI36
NG_016290.1:g.63715T>C
NG_016290.2:g.64940T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367921.8:c.-27-27885T>C MANE Select ENSP00000356898.3:n.-27-27885T>C
ENST00000446985.6:c.-27-27885T>C ENSP00000400309.2:n.-27-27885T>C
ENST00000671979.1:c.-107-13900T>C ENSP00000500822.1:n.-107-13900T>C
ENST00000672207.1:n.360-27885T>C
ENST00000673239.1:n.463+13806T>C
ENST00000367921.7:c.-27-27885T>C ENSP00000356898.3:n.-27-27885T>C
ENST00000367922.7:c.-107-13900T>C ENSP00000356899.2:n.-107-13900T>C
ENST00000415555.5:c.-27-27885T>C ENSP00000391310.1:n.-27-27885T>C
ENST00000446985.5:c.-27-27885T>C ENSP00000400309.1:n.-27-27885T>C
NM_001014796.1:c.-107-13900T>C NP_001014796.1:n.-107-13900T>C
NM_006182.2:c.-27-27885T>C NP_006173.2:n.-27-27885T>C
XM_006711344.2:c.-27-27885T>C XP_006711407.1:n.-27-27885T>C
XM_011509586.1:c.-27-27885T>C XP_011507888.1:n.-27-27885T>C
XM_011509587.1:c.-107-13900T>C XP_011507889.1:n.-107-13900T>C
NM_001014796.2:c.-107-13900T>C NP_001014796.1:n.-107-13900T>C
NM_001354982.1:c.-27-27885T>C NP_001341911.1:n.-27-27885T>C
NM_001354983.1:c.-27-27885T>C NP_001341912.1:n.-27-27885T>C
NM_006182.3:c.-27-27885T>C NP_006173.2:n.-27-27885T>C
XM_011509587.2:c.-107-13900T>C XP_011507889.1:n.-107-13900T>C
XM_011509588.3:c.-27-27885T>C XP_011507890.1:n.-27-27885T>C
NM_006182.4:c.-27-27885T>C MANE Select NP_006173.2:n.-27-27885T>C
NM_001014796.3:c.-107-13900T>C NP_001014796.1:n.-107-13900T>C
NM_001354982.2:c.-27-27885T>C NP_001341911.1:n.-27-27885T>C
NM_001354983.2:c.-27-27885T>C NP_001341912.1:n.-27-27885T>C