Canonical Allele Identifier: CA1008513784
Gene: DDR2 HGNC NCBI

Linked Data

dbSNP Id: rs1659946679

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162691174G>A , CM000663.2:g.162691174G>A GRCh38
NC_000001.10:g.162660964G>A , CM000663.1:g.162660964G>A GRCh37
NC_000001.9:g.160927588G>A NCBI36
NG_016290.1:g.63737G>A
NG_016290.2:g.64962G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367921.8:c.-27-27863G>A MANE Select ENSP00000356898.3:n.-27-27863G>A
ENST00000446985.6:c.-27-27863G>A ENSP00000400309.2:n.-27-27863G>A
ENST00000671979.1:c.-107-13878G>A ENSP00000500822.1:n.-107-13878G>A
ENST00000672207.1:n.360-27863G>A
ENST00000673239.1:n.463+13828G>A
ENST00000367921.7:c.-27-27863G>A ENSP00000356898.3:n.-27-27863G>A
ENST00000367922.7:c.-107-13878G>A ENSP00000356899.2:n.-107-13878G>A
ENST00000415555.5:c.-27-27863G>A ENSP00000391310.1:n.-27-27863G>A
ENST00000446985.5:c.-27-27863G>A ENSP00000400309.1:n.-27-27863G>A
NM_001014796.1:c.-107-13878G>A NP_001014796.1:n.-107-13878G>A
NM_006182.2:c.-27-27863G>A NP_006173.2:n.-27-27863G>A
XM_006711344.2:c.-27-27863G>A XP_006711407.1:n.-27-27863G>A
XM_011509586.1:c.-27-27863G>A XP_011507888.1:n.-27-27863G>A
XM_011509587.1:c.-107-13878G>A XP_011507889.1:n.-107-13878G>A
NM_001014796.2:c.-107-13878G>A NP_001014796.1:n.-107-13878G>A
NM_001354982.1:c.-27-27863G>A NP_001341911.1:n.-27-27863G>A
NM_001354983.1:c.-27-27863G>A NP_001341912.1:n.-27-27863G>A
NM_006182.3:c.-27-27863G>A NP_006173.2:n.-27-27863G>A
XM_011509587.2:c.-107-13878G>A XP_011507889.1:n.-107-13878G>A
XM_011509588.3:c.-27-27863G>A XP_011507890.1:n.-27-27863G>A
NM_006182.4:c.-27-27863G>A MANE Select NP_006173.2:n.-27-27863G>A
NM_001014796.3:c.-107-13878G>A NP_001014796.1:n.-107-13878G>A
NM_001354982.2:c.-27-27863G>A NP_001341911.1:n.-27-27863G>A
NM_001354983.2:c.-27-27863G>A NP_001341912.1:n.-27-27863G>A