Canonical Allele Identifier: CA3704732
Gene: DDR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1049623

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30897052T>C , CM000668.2:g.30897052T>C GRCh38
NC_000006.11:g.30864829T>C , CM000668.1:g.30864829T>C GRCh37
NC_000006.10:g.30972808T>C NCBI36
NG_029066.1:g.17969T>C

Transcript Alleles

HGVS Amino-acid change
NM_001202521.1:c.*25T>C VV NP_001189450.1:p.=
NM_001202522.1:c.1470T>C VV NP_001189451.1:p.Val490=
NM_001202523.1:c.1851T>C VV NP_001189452.1:p.Val617=
NM_001297652.1:c.1797T>C VV NP_001284581.1:p.Val599=
NM_001297653.1:c.1797T>C VV NP_001284582.1:p.Val599=
NM_001297654.1:c.1908T>C VV NP_001284583.1:p.Val636=
NM_001954.4:c.1797T>C VV NP_001945.3:p.Val599=
NM_013993.2:c.1908T>C VV NP_054699.2:p.Val636=
NM_013994.2:c.1908T>C VV NP_054700.2:p.Val636=
XM_006715185.1:c.1962T>C XP_006715248.1:p.Val654=
XM_011514882.1:c.1962T>C XP_011513184.1:p.Val654=
XM_011514883.1:c.1908T>C XP_011513185.1:p.Val636=
XM_011514884.1:c.1908T>C XP_011513186.1:p.Val636=
XM_011514885.1:c.1908T>C XP_011513187.1:p.Val636=
XM_011514886.1:c.1908T>C XP_011513188.1:p.Val636=
XM_011514887.1:c.1908T>C XP_011513189.1:p.Val636=
XM_011514888.1:c.1851T>C XP_011513190.1:p.Val617=
XM_006715185.2:c.1962T>C
XM_011514882.2:c.1962T>C
XM_011514883.2:c.1908T>C
XM_011514885.2:c.1908T>C
XM_011514886.2:c.1908T>C
XM_011514887.2:c.1908T>C
XM_011514888.3:c.1851T>C
XM_017011268.2:c.1908T>C XP_016866757.1:p.Val636=
XM_017011269.2:c.1797T>C XP_016866758.1:p.Val599=
XM_024446540.1:c.1908T>C XP_024302308.1:p.Val636=
XM_024446541.1:c.1908T>C XP_024302309.1:p.Val636=
XM_024446542.1:c.1908T>C XP_024302310.1:p.Val636=
ENST00000324771.12:c.1908T>C ENSP00000318217.8:p.Val636=
ENST00000376567.6:c.1797T>C ENSP00000365751.2:p.Val599=
ENST00000376568.7:c.1908T>C ENSP00000365752.3:p.Val636=
ENST00000376569.7:c.1797T>C ENSP00000365753.3:p.Val599=
ENST00000376570.8:c.1797T>C ENSP00000365754.4:p.Val599=
ENST00000417521.5:n.1104T>C ENSP00000398682.1:p.Val368=
ENST00000418800.6:c.1797T>C ENSP00000407699.2:p.Val599=
ENST00000446312.5:c.1470T>C ENSP00000405998.2:p.Val490=
ENST00000452441.5:c.1908T>C ENSP00000405039.1:p.Val636=
ENST00000454612.6:c.1797T>C ENSP00000406091.2:p.Val599=
ENST00000482873.6:c.*965T>C ENSP00000421978.1:p.=
ENST00000508312.5:c.1851T>C ENSP00000422442.1:p.Val617=
ENST00000513240.5:n.1908T>C ENSP00000427552.1:p.Val636=
ENST00000514434.1:n.382T>C