Canonical Allele Identifier: CA363126242

Gene: DDR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30884156G>T , CM000668.2:g.30884156G>T	GRCh38
NC_000006.11:g.30851933G>T , CM000668.1:g.30851933G>T	GRCh37
NC_000006.10:g.30959912G>T	NCBI36
NG_029066.1:g.5073G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324771.12:c.-271-382G>T	ENSP00000318217.8:n.-271-382G>T
ENST00000376569.7:c.-216+11G>T	ENSP00000365753.3:n.-216+11G>T
ENST00000376570.8:c.-272+11G>T	ENSP00000365754.4:n.-272+11G>T
ENST00000396342.6:c.-43+991G>T	ENSP00000379631.2:n.-43+991G>T
ENST00000412274.6:c.-271-382G>T	ENSP00000392413.2:n.-271-382G>T
ENST00000418800.6:c.-43+1173G>T	ENSP00000407699.2:n.-43+1173G>T
ENST00000437124.6:c.-99+1173G>T	ENSP00000394273.2:n.-99+1173G>T
ENST00000454612.6:c.-272+11G>T	ENSP00000406091.2:n.-272+11G>T
ENST00000460944.6:c.-43+3031G>T	ENSP00000426420.1:n.-43+3031G>T
ENST00000482050.1:n.77-382G>T
ENST00000502955.5:c.-43+3031G>T	ENSP00000424346.1:n.-43+3031G>T
ENST00000503180.5:c.-215-382G>T	ENSP00000424468.1:n.-215-382G>T
ENST00000503628.5:c.-43+915G>T	ENSP00000426799.1:n.-43+915G>T
ENST00000504651.5:c.-271-382G>T	ENSP00000424758.1:n.-271-382G>T
ENST00000504927.5:c.-20+11G>T	ENSP00000427597.1:n.-20+11G>T
ENST00000505066.5:c.-42-4532G>T	ENSP00000421189.1:n.-42-4532G>T
ENST00000505534.5:c.-215-382G>T	ENSP00000420833.1:n.-215-382G>T
ENST00000507046.5:c.-271-382G>T	ENSP00000425713.1:n.-271-382G>T
ENST00000507901.5:c.-215-382G>T	ENSP00000424703.1:n.-215-382G>T
ENST00000508317.5:c.-98-1469G>T	ENSP00000427369.1:n.-98-1469G>T
ENST00000509639.5:c.-215-382G>T	ENSP00000422331.1:n.-215-382G>T
ENST00000511510.5:c.-43+11G>T	ENSP00000425113.1:n.-43+11G>T
ENST00000512694.5:c.-43+915G>T	ENSP00000426229.1:n.-43+915G>T
ENST00000513043.5:c.-272+269G>T	ENSP00000423928.1:n.-272+269G>T
ENST00000513749.5:c.-43+3031G>T	ENSP00000421753.1:n.-43+3031G>T
ENST00000515233.5:c.-43+833G>T	ENSP00000422467.1:n.-43+833G>T
ENST00000515529.4:n.51-382G>T
ENST00000515881.5:c.-216+227G>T	ENSP00000423492.1:n.-216+227G>T
NM_001297652.1:c.-43+1173G>T	NP_001284581.1:n.-43+1173G>T
NM_001954.4:c.-272+11G>T	NP_001945.3:n.-272+11G>T
XM_011514883.1:c.-271-382G>T	XP_011513185.1:n.-271-382G>T
XM_011514884.1:c.-271-382G>T	XP_011513186.1:n.-271-382G>T
XM_011514886.1:c.-43+1173G>T	XP_011513188.1:n.-43+1173G>T
XM_011514887.1:c.-43+3031G>T	XP_011513189.1:n.-43+3031G>T
XM_011514883.2:c.-271-382G>T	XP_011513185.1:n.-271-382G>T
XM_011514886.2:c.-43+1173G>T	XP_011513188.1:n.-43+1173G>T
XM_011514887.2:c.-43+3031G>T	XP_011513189.1:n.-43+3031G>T
XM_017011268.2:c.-43+915G>T	XP_016866757.1:n.-43+915G>T
XM_017011269.2:c.-43+3031G>T	XP_016866758.1:n.-43+3031G>T
XM_024446541.1:c.-43+991G>T	XP_024302309.1:n.-43+991G>T
XM_024446542.1:c.-43+991G>T	XP_024302310.1:n.-43+991G>T
NM_001297652.2:c.-43+1173G>T	NP_001284581.1:n.-43+1173G>T
NM_001387892.1:c.-43+1173G>T	NP_001374821.1:n.-43+1173G>T
NM_001387893.1:c.-43+3031G>T	NP_001374822.1:n.-43+3031G>T
NM_001387894.1:c.-215-382G>T	NP_001374823.1:n.-215-382G>T
NM_001387895.1:c.-272+11G>T	NP_001374824.1:n.-272+11G>T
NM_001387897.1:c.-271-382G>T	NP_001374826.1:n.-271-382G>T
NM_001387898.1:c.-43+11G>T	NP_001374827.1:n.-43+11G>T
NM_001387899.1:c.-271-382G>T	NP_001374828.1:n.-271-382G>T
NM_001387900.1:c.-43+1173G>T	NP_001374829.1:n.-43+1173G>T
NM_001387901.1:c.-271-382G>T	NP_001374830.1:n.-271-382G>T
NM_001387902.1:c.-216+11G>T	NP_001374831.1:n.-216+11G>T
NM_001387903.1:c.-466+11G>T	NP_001374832.1:n.-466+11G>T
NM_001387904.1:c.-99+11G>T	NP_001374833.1:n.-99+11G>T
NM_001387905.1:c.-43+1173G>T	NP_001374834.1:n.-43+1173G>T
NM_001387907.1:c.-43+11G>T	NP_001374836.1:n.-43+11G>T
NM_001387908.1:c.-43+3031G>T	NP_001374837.1:n.-43+3031G>T
NM_001387909.1:c.-98-1469G>T	NP_001374838.1:n.-98-1469G>T
NM_001387910.1:c.-99+1173G>T	NP_001374839.1:n.-99+1173G>T
NM_001387911.1:c.-99+991G>T	NP_001374840.1:n.-99+991G>T
NM_001387912.1:c.-43+991G>T	NP_001374841.1:n.-43+991G>T
NM_001387913.1:c.-43+11G>T	NP_001374842.1:n.-43+11G>T
NM_001387914.1:c.-216+11G>T	NP_001374843.1:n.-216+11G>T
NM_001387915.1:c.-271-382G>T	NP_001374844.1:n.-271-382G>T
NM_001387917.1:c.-272+227G>T	NP_001374846.1:n.-272+227G>T
NM_001387918.1:c.-215-382G>T	NP_001374847.1:n.-215-382G>T
NM_001954.5:c.-272+11G>T	NP_001945.3:n.-272+11G>T