Canonical Allele Identifier: CA1411096370

Gene: MED12L P2RY12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151382537_151382541delinsCTTTG , CM000665.2:g.151382537_151382541delinsCTTTG	GRCh38
NC_000003.11:g.151100325_151100329delinsCTTTG , CM000665.1:g.151100325_151100329delinsCTTTG	GRCh37
NC_000003.10:g.152583015_152583019delinsCTTTG	NCBI36
NG_016019.1:g.7216_7220delinsCAAAG , LRG_569:g.7216_7220delinsCAAAG
NG_021244.1:g.300650_300654delinsCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686666.1:c.4204-119_4204-115delinsCTTTG (MED12L)	ENSP00000509482.1:n.4204-119_4204-115delinsCTTTG
ENST00000687756.1:c.4591-119_4591-115delinsCTTTG (MED12L) MANE Select	ENSP00000508695.1:n.4591-119_4591-115delinsCTTTG
ENST00000302632.4:c.-180+2151_-180+2155delinsCAAAG (P2RY12) MANE Select	ENSP00000307259.4:n.-180+2151_-180+2155delinsCAAAG
ENST00000273432.8:c.4066-119_4066-115delinsCTTTG (MED12L)	ENSP00000273432.4:n.4066-119_4066-115delinsCTTTG
ENST00000302632.3:c.-180+2151_-180+2155delinsCAAAG (P2RY12)	ENSP00000307259.3:n.-180+2151_-180+2155delinsCAAAG
ENST00000474524.5:c.4486-119_4486-115delinsCTTTG (MED12L)	ENSP00000417235.1:n.4486-119_4486-115delinsCTTTG
NM_022788.4:c.-180+2151_-180+2155delinsCAAAG , LRG_569t1:c.-180+2151_-180+2155delinsCAAAG (P2RY12)	NP_073625.1:n.-180+2151_-180+2155delinsCAAAG
NM_053002.5:c.4486-119_4486-115delinsCTTTG (MED12L)	NP_443728.3:n.4486-119_4486-115delinsCTTTG
XM_006713487.2:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_006713550.1:n.4591-119_4591-115delinsCTTTG
XM_011512386.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510688.1:n.4591-119_4591-115delinsCTTTG
XM_011512387.1:c.4588-119_4588-115delinsCTTTG (MED12L)	XP_011510689.1:n.4588-119_4588-115delinsCTTTG
XM_011512388.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510690.1:n.4591-119_4591-115delinsCTTTG
XM_011512389.1:c.4486-119_4486-115delinsCTTTG (MED12L)	XP_011510691.1:n.4486-119_4486-115delinsCTTTG
XM_011512390.1:c.4486-119_4486-115delinsCTTTG (MED12L)	XP_011510692.1:n.4486-119_4486-115delinsCTTTG
XM_011512391.1:c.4321-119_4321-115delinsCTTTG (MED12L)	XP_011510693.1:n.4321-119_4321-115delinsCTTTG
XM_011512392.1:c.4135-119_4135-115delinsCTTTG (MED12L)	XP_011510694.1:n.4135-119_4135-115delinsCTTTG
XM_011512393.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510695.1:n.4591-119_4591-115delinsCTTTG
XM_011512394.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510696.1:n.4591-119_4591-115delinsCTTTG
XM_011512395.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510697.1:n.4591-119_4591-115delinsCTTTG
XM_011512396.1:c.3016-119_3016-115delinsCTTTG (MED12L)	XP_011510698.1:n.3016-119_3016-115delinsCTTTG
XM_011512397.1:c.2458-119_2458-115delinsCTTTG (MED12L)	XP_011510699.1:n.2458-119_2458-115delinsCTTTG
XM_011512398.1:c.2386-119_2386-115delinsCTTTG (MED12L)	XP_011510700.1:n.2386-119_2386-115delinsCTTTG
XM_011512400.1:c.1408-119_1408-115delinsCTTTG (MED12L)	XP_011510702.1:n.1408-119_1408-115delinsCTTTG
XM_006713487.3:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_006713550.1:n.4591-119_4591-115delinsCTTTG
XM_011512390.2:c.4486-119_4486-115delinsCTTTG (MED12L)	XP_011510692.1:n.4486-119_4486-115delinsCTTTG
XM_011512394.2:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_011510696.1:n.4591-119_4591-115delinsCTTTG
XM_017005676.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_016861165.1:n.4591-119_4591-115delinsCTTTG
XM_017005677.1:c.4588-119_4588-115delinsCTTTG (MED12L)	XP_016861166.1:n.4588-119_4588-115delinsCTTTG
XM_017005678.1:c.4591-119_4591-115delinsCTTTG (MED12L)	XP_016861167.1:n.4591-119_4591-115delinsCTTTG
XM_017005679.1:c.4321-119_4321-115delinsCTTTG (MED12L)	XP_016861168.1:n.4321-119_4321-115delinsCTTTG
XM_017005680.1:c.4309-119_4309-115delinsCTTTG (MED12L)	XP_016861169.1:n.4309-119_4309-115delinsCTTTG
XM_017005681.1:c.1978-119_1978-115delinsCTTTG (MED12L)	XP_016861170.1:n.1978-119_1978-115delinsCTTTG
XR_001740000.1:n.4992-119_4992-115delinsCTTTG (MED12L)
NM_022788.5:c.-180+2151_-180+2155delinsCAAAG (P2RY12) MANE Select	NP_073625.1:n.-180+2151_-180+2155delinsCAAAG
NM_001393769.1:c.4591-119_4591-115delinsCTTTG (MED12L) MANE Select	NP_001380698.1:n.4591-119_4591-115delinsCTTTG
NM_053002.6:c.4486-119_4486-115delinsCTTTG (MED12L)	NP_443728.3:n.4486-119_4486-115delinsCTTTG