Canonical Allele Identifier: CA10637810

Gene: DPAGT1

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119096581A>G , CM000673.2:g.119096581A>G	GRCh38
NC_000011.9:g.118967291A>G , CM000673.1:g.118967291A>G	GRCh37
NC_000011.8:g.118472501A>G	NCBI36
NG_008918.1:g.10495T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1868T>C
ENST00000524658.2:n.1927T>C
ENST00000530052.2:n.2933T>C
ENST00000682191.1:n.2227T>C
ENST00000682192.1:n.2090T>C
ENST00000682232.1:c.*1261T>C	ENSP00000507302.1:n.*1261T>C
ENST00000682326.1:c.*614T>C	ENSP00000508129.1:n.*614T>C
ENST00000682517.1:n.3214T>C
ENST00000682652.1:n.2996T>C
ENST00000682665.1:n.2588T>C
ENST00000682691.1:n.2510T>C
ENST00000682791.1:c.*417T>C	ENSP00000507312.1:n.*417T>C
ENST00000682811.1:c.*695T>C	ENSP00000508196.1:n.*695T>C
ENST00000682946.1:c.*726T>C	ENSP00000506856.1:n.*726T>C
ENST00000683143.1:c.*1349T>C	ENSP00000507168.1:n.*1349T>C
ENST00000683373.1:n.2149T>C
ENST00000683558.1:n.2393T>C
ENST00000683567.1:n.1753T>C
ENST00000683955.1:n.2400T>C
ENST00000684142.1:c.*1485T>C	ENSP00000508008.1:n.*1485T>C
ENST00000684252.1:n.2285T>C
ENST00000684255.1:c.*1515T>C	ENSP00000507398.1:n.*1515T>C
ENST00000684315.1:n.2455T>C
ENST00000684345.1:c.*1788T>C	ENSP00000507163.1:n.*1788T>C
ENST00000684499.1:c.*1915T>C	ENSP00000506800.1:n.*1915T>C
ENST00000684682.1:c.*1619T>C	ENSP00000507326.1:n.*1619T>C
ENST00000354202.9:c.*417T>C MANE Select	ENSP00000346142.4:n.*417T>C
ENST00000354202.8:c.*417T>C	ENSP00000346142.4:n.*417T>C
ENST00000392834.7:c.*1349T>C	ENSP00000376579.3:n.*1349T>C
ENST00000409993.6:c.*417T>C	ENSP00000386597.2:n.*417T>C
ENST00000414373.5:c.*1113T>C	ENSP00000402019.1:n.*1113T>C
ENST00000461999.1:n.2055T>C
ENST00000481084.5:n.2273T>C
NM_001382.3:c.*417T>C	NP_001373.2:n.*417T>C
XM_005271422.2:c.*417T>C	XP_005271479.1:n.*417T>C
XM_011542648.1:c.*417T>C	XP_011540950.1:n.*417T>C
XR_947801.1:n.1803T>C
XM_005271422.3:c.*417T>C	XP_005271479.1:n.*417T>C
XM_011542648.2:c.*417T>C	XP_011540950.1:n.*417T>C
XM_017017293.2:c.*417T>C	XP_016872782.1:n.*417T>C
XM_017017294.2:c.*970T>C	XP_016872783.1:n.*970T>C
XM_017017295.1:c.*417T>C	XP_016872784.1:n.*417T>C
XR_001747785.2:n.1678T>C
XR_947801.2:n.1590T>C
NM_001382.4:c.*417T>C MANE Select	NP_001373.2:n.*417T>C