Canonical Allele Identifier: CA2725107993

Gene: DPAGT1

Linked Data

• dbSNP Id: rs2134911315

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100409_119100410insCAAG , CM000673.2:g.119100409_119100410insCAAG	GRCh38
NC_000011.9:g.118971119_118971120insCAAG , CM000673.1:g.118971119_118971120insCAAG	GRCh37
NC_000011.8:g.118476329_118476330insCAAG	NCBI36
NG_008918.1:g.6666_6667insCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.673-2_673-1insCTTG
ENST00000530052.2:n.1239-2_1239-1insCTTG
ENST00000682191.1:n.699-2_699-1insCTTG
ENST00000682192.1:n.699-2_699-1insCTTG
ENST00000682232.1:c.*202-2_*202-1insCTTG	ENSP00000507302.1:n.*202-2_*202-1insCTTG
ENST00000682326.1:c.497-2_497-1insCTTG	ENSP00000508129.1:n.497-2_497-1insCTTG
ENST00000682404.1:n.1239-2_1239-1insCTTG
ENST00000682517.1:n.1239-2_1239-1insCTTG
ENST00000682652.1:n.1468-2_1468-1insCTTG
ENST00000682665.1:n.894-2_894-1insCTTG
ENST00000682691.1:n.894-2_894-1insCTTG
ENST00000682791.1:c.410-2_410-1insCTTG	ENSP00000507312.1:n.410-2_410-1insCTTG
ENST00000682811.1:c.497-2_497-1insCTTG	ENSP00000508196.1:n.497-2_497-1insCTTG
ENST00000682883.1:n.800-2_800-1insCTTG
ENST00000682946.1:c.497-2_497-1insCTTG	ENSP00000506856.1:n.497-2_497-1insCTTG
ENST00000683143.1:c.*202-2_*202-1insCTTG	ENSP00000507168.1:n.*202-2_*202-1insCTTG
ENST00000683373.1:n.699-2_699-1insCTTG
ENST00000683558.1:n.699-2_699-1insCTTG
ENST00000683567.1:n.724-2_724-1insCTTG
ENST00000683955.1:n.894-2_894-1insCTTG
ENST00000684142.1:c.*172-2_*172-1insCTTG	ENSP00000508008.1:n.*172-2_*172-1insCTTG
ENST00000684252.1:n.894-2_894-1insCTTG
ENST00000684255.1:c.*202-2_*202-1insCTTG	ENSP00000507398.1:n.*202-2_*202-1insCTTG
ENST00000684315.1:n.1230-2_1230-1insCTTG
ENST00000684345.1:c.*172-2_*172-1insCTTG	ENSP00000507163.1:n.*172-2_*172-1insCTTG
ENST00000684499.1:c.*602-2_*602-1insCTTG	ENSP00000506800.1:n.*602-2_*602-1insCTTG
ENST00000684682.1:c.162-2_162-1insCTTG	ENSP00000507326.1:n.162-2_162-1insCTTG
ENST00000354202.9:c.497-2_497-1insCTTG MANE Select	ENSP00000346142.4:n.497-2_497-1insCTTG
ENST00000639704.1:c.404-2_404-1insCTTG	ENSP00000491336.1:n.404-2_404-1insCTTG
ENST00000640102.1:c.*150-2_*150-1insCTTG	ENSP00000492027.1:n.*150-2_*150-1insCTTG
ENST00000640747.1:c.*172-2_*172-1insCTTG	ENSP00000492730.1:n.*172-2_*172-1insCTTG
ENST00000354202.8:c.497-2_497-1insCTTG	ENSP00000346142.4:n.497-2_497-1insCTTG
ENST00000392834.7:c.*202-2_*202-1insCTTG	ENSP00000376579.3:n.*202-2_*202-1insCTTG
ENST00000409993.6:c.497-2_497-1insCTTG	ENSP00000386597.2:n.497-2_497-1insCTTG
ENST00000414373.5:c.*243-2_*243-1insCTTG	ENSP00000402019.1:n.*243-2_*243-1insCTTG
ENST00000442480.1:c.347-2_347-1insCTTG	ENSP00000406591.1:n.347-2_347-1insCTTG
ENST00000481084.5:n.1126-2_1126-1insCTTG
ENST00000525456.5:n.500-2_500-1insCTTG
ENST00000530052.1:n.395-2_395-1insCTTG
ENST00000533687.1:n.507_508insCTTG
NM_001382.3:c.497-2_497-1insCTTG	NP_001373.2:n.497-2_497-1insCTTG
XM_005271422.2:c.497-2_497-1insCTTG	XP_005271479.1:n.497-2_497-1insCTTG
XM_011542648.1:c.176-2_176-1insCTTG	XP_011540950.1:n.176-2_176-1insCTTG
XR_947801.1:n.933-2_933-1insCTTG
XM_005271422.3:c.497-2_497-1insCTTG	XP_005271479.1:n.497-2_497-1insCTTG
XM_011542648.2:c.176-2_176-1insCTTG	XP_011540950.1:n.176-2_176-1insCTTG
XM_017017293.2:c.176-2_176-1insCTTG	XP_016872782.1:n.176-2_176-1insCTTG
XM_017017294.2:c.497-2_497-1insCTTG	XP_016872783.1:n.497-2_497-1insCTTG
XM_017017295.1:c.-20-2_-20-1insCTTG	XP_016872784.1:n.-20-2_-20-1insCTTG
XR_001747785.2:n.720-2_720-1insCTTG
XR_947801.2:n.720-2_720-1insCTTG
NM_001382.4:c.497-2_497-1insCTTG MANE Select	NP_001373.2:n.497-2_497-1insCTTG