Canonical Allele Identifier: CA890314574
Gene: DDR2 HGNC NCBI

Linked Data

dbSNP Id: rs1246269580

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.162691168dup , CM000663.2:g.162691168dup GRCh38
NC_000001.10:g.162660958dup , CM000663.1:g.162660958dup GRCh37
NC_000001.9:g.160927582dup NCBI36
NG_016290.1:g.63731dup
NG_016290.2:g.64956dup

Transcript Alleles

HGVS Amino-acid change
ENST00000367921.8:c.-27-27869dup MANE Select ENSP00000356898.3:n.-27-27869dup
ENST00000446985.6:c.-27-27869dup ENSP00000400309.2:n.-27-27869dup
ENST00000671979.1:c.-107-13884dup ENSP00000500822.1:n.-107-13884dup
ENST00000672207.1:n.360-27869dup
ENST00000673239.1:n.463+13822dup
ENST00000367921.7:c.-27-27869dup ENSP00000356898.3:n.-27-27869dup
ENST00000367922.7:c.-107-13884dup ENSP00000356899.2:n.-107-13884dup
ENST00000415555.5:c.-27-27869dup ENSP00000391310.1:n.-27-27869dup
ENST00000446985.5:c.-27-27869dup ENSP00000400309.1:n.-27-27869dup
NM_001014796.1:c.-107-13884dup NP_001014796.1:n.-107-13884dup
NM_006182.2:c.-27-27869dup NP_006173.2:n.-27-27869dup
XM_006711344.2:c.-27-27869dup XP_006711407.1:n.-27-27869dup
XM_011509586.1:c.-27-27869dup XP_011507888.1:n.-27-27869dup
XM_011509587.1:c.-107-13884dup XP_011507889.1:n.-107-13884dup
NM_001014796.2:c.-107-13884dup NP_001014796.1:n.-107-13884dup
NM_001354982.1:c.-27-27869dup NP_001341911.1:n.-27-27869dup
NM_001354983.1:c.-27-27869dup NP_001341912.1:n.-27-27869dup
NM_006182.3:c.-27-27869dup NP_006173.2:n.-27-27869dup
XM_011509587.2:c.-107-13884dup XP_011507889.1:n.-107-13884dup
XM_011509588.3:c.-27-27869dup XP_011507890.1:n.-27-27869dup
NM_006182.4:c.-27-27869dup MANE Select NP_006173.2:n.-27-27869dup
NM_001014796.3:c.-107-13884dup NP_001014796.1:n.-107-13884dup
NM_001354982.2:c.-27-27869dup NP_001341911.1:n.-27-27869dup
NM_001354983.2:c.-27-27869dup NP_001341912.1:n.-27-27869dup