Canonical Allele Identifier: CA15461365
Gene: DDR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1049633

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30899750G>A , CM000668.2:g.30899750G>A GRCh38
NC_000006.10:g.30975506G>A NCBI36
NC_000006.11:g.30867527G>A , CM000668.1:g.30867527G>A GRCh37
NG_029066.1:g.20667G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000324771.12:c.*454G>A ENSP00000318217.8:p.=
ENST00000376567.6:c.*454G>A ENSP00000365751.2:p.=
ENST00000376568.7:c.*454G>A ENSP00000365752.3:p.=
ENST00000376569.7:c.*454G>A ENSP00000365753.3:p.=
ENST00000376570.8:c.*454G>A ENSP00000365754.4:p.=
ENST00000418800.6:c.*454G>A ENSP00000407699.2:p.=
ENST00000446312.5:c.*454G>A ENSP00000405998.2:p.=
ENST00000452441.5:c.*454G>A ENSP00000405039.1:p.=
ENST00000454612.6:c.*454G>A ENSP00000406091.2:p.=
NM_001202521.1:c.*1313G>A VV NP_001189450.1:p.=
NM_001202522.1:c.*454G>A VV NP_001189451.1:p.=
NM_001202523.1:c.*454G>A VV NP_001189452.1:p.=
NM_001297652.1:c.*454G>A VV NP_001284581.1:p.=
NM_001297653.1:c.*454G>A VV NP_001284582.1:p.=
NM_001297654.1:c.*454G>A VV NP_001284583.1:p.=
NM_001954.4:c.*454G>A VV NP_001945.3:p.=
NM_013993.2:c.*454G>A VV NP_054699.2:p.=
NM_013994.2:c.*454G>A VV NP_054700.2:p.=
XM_006715185.1:c.*454G>A XP_006715248.1:p.=
XM_011514882.1:c.*454G>A XP_011513184.1:p.=
XM_011514883.1:c.*454G>A XP_011513185.1:p.=
XM_011514884.1:c.*454G>A XP_011513186.1:p.=
XM_011514885.1:c.*454G>A XP_011513187.1:p.=
XM_011514886.1:c.*454G>A XP_011513188.1:p.=
XM_011514887.1:c.*454G>A XP_011513189.1:p.=
XM_011514888.1:c.*454G>A XP_011513190.1:p.=