Canonical Allele Identifier: CA2830535545

Gene: MED12L P2RY12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151360671_151360672insACA , CM000665.2:g.151360671_151360672insACA	GRCh38
NC_000003.11:g.151078459_151078460insACA , CM000665.1:g.151078459_151078460insACA	GRCh37
NC_000003.10:g.152561149_152561150insACA	NCBI36
NG_016019.1:g.29086_29087insGTT , LRG_569:g.29086_29087insGTT
NG_021244.1:g.278784_278785insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686666.1:c.2570+66_2570+67insACA (MED12L)	ENSP00000509482.1:n.2570+66_2570+67insACA
ENST00000687756.1:c.2957+66_2957+67insACA (MED12L) MANE Select	ENSP00000508695.1:n.2957+66_2957+67insACA
ENST00000302632.4:c.-179-19911_-179-19910insGTT (P2RY12) MANE Select	ENSP00000307259.4:n.-179-19911_-179-19910insGTT
ENST00000273432.8:c.2432+66_2432+67insACA (MED12L)	ENSP00000273432.4:n.2432+66_2432+67insACA
ENST00000302632.3:c.-179-19911_-179-19910insGTT (P2RY12)	ENSP00000307259.3:n.-179-19911_-179-19910insGTT
ENST00000474524.5:c.2852+66_2852+67insACA (MED12L)	ENSP00000417235.1:n.2852+66_2852+67insACA
NM_022788.4:c.-179-19911_-179-19910insGTT , LRG_569t1:c.-179-19911_-179-19910insGTT (P2RY12)	NP_073625.1:n.-179-19911_-179-19910insGTT
NM_053002.5:c.2852+66_2852+67insACA (MED12L)	NP_443728.3:n.2852+66_2852+67insACA
XM_006713487.2:c.2957+66_2957+67insACA (MED12L)	XP_006713550.1:n.2957+66_2957+67insACA
XM_011512386.1:c.2957+66_2957+67insACA (MED12L)	XP_011510688.1:n.2957+66_2957+67insACA
XM_011512387.1:c.2957+66_2957+67insACA (MED12L)	XP_011510689.1:n.2957+66_2957+67insACA
XM_011512388.1:c.2957+66_2957+67insACA (MED12L)	XP_011510690.1:n.2957+66_2957+67insACA
XM_011512389.1:c.2852+66_2852+67insACA (MED12L)	XP_011510691.1:n.2852+66_2852+67insACA
XM_011512390.1:c.2852+66_2852+67insACA (MED12L)	XP_011510692.1:n.2852+66_2852+67insACA
XM_011512391.1:c.2687+66_2687+67insACA (MED12L)	XP_011510693.1:n.2687+66_2687+67insACA
XM_011512392.1:c.2501+66_2501+67insACA (MED12L)	XP_011510694.1:n.2501+66_2501+67insACA
XM_011512393.1:c.2957+66_2957+67insACA (MED12L)	XP_011510695.1:n.2957+66_2957+67insACA
XM_011512394.1:c.2957+66_2957+67insACA (MED12L)	XP_011510696.1:n.2957+66_2957+67insACA
XM_011512395.1:c.2957+66_2957+67insACA (MED12L)	XP_011510697.1:n.2957+66_2957+67insACA
XM_011512396.1:c.1382+66_1382+67insACA (MED12L)	XP_011510698.1:n.1382+66_1382+67insACA
XM_011512397.1:c.824+66_824+67insACA (MED12L)	XP_011510699.1:n.824+66_824+67insACA
XM_011512398.1:c.752+66_752+67insACA (MED12L)	XP_011510700.1:n.752+66_752+67insACA
XM_011512399.1:c.2957+66_2957+67insACA (MED12L)	XP_011510701.1:n.2957+66_2957+67insACA
XM_006713487.3:c.2957+66_2957+67insACA (MED12L)	XP_006713550.1:n.2957+66_2957+67insACA
XM_011512390.2:c.2852+66_2852+67insACA (MED12L)	XP_011510692.1:n.2852+66_2852+67insACA
XM_011512394.2:c.2957+66_2957+67insACA (MED12L)	XP_011510696.1:n.2957+66_2957+67insACA
XM_011512399.3:c.2957+66_2957+67insACA (MED12L)	XP_011510701.1:n.2957+66_2957+67insACA
XM_017005676.1:c.2957+66_2957+67insACA (MED12L)	XP_016861165.1:n.2957+66_2957+67insACA
XM_017005677.1:c.2957+66_2957+67insACA (MED12L)	XP_016861166.1:n.2957+66_2957+67insACA
XM_017005678.1:c.2957+66_2957+67insACA (MED12L)	XP_016861167.1:n.2957+66_2957+67insACA
XM_017005679.1:c.2687+66_2687+67insACA (MED12L)	XP_016861168.1:n.2687+66_2687+67insACA
XM_017005680.1:c.2675+66_2675+67insACA (MED12L)	XP_016861169.1:n.2675+66_2675+67insACA
XM_017005681.1:c.344+66_344+67insACA (MED12L)	XP_016861170.1:n.344+66_344+67insACA
XR_001740000.1:n.3358+66_3358+67insACA (MED12L)
NM_022788.5:c.-179-19911_-179-19910insGTT (P2RY12) MANE Select	NP_073625.1:n.-179-19911_-179-19910insGTT
NM_001393769.1:c.2957+66_2957+67insACA (MED12L) MANE Select	NP_001380698.1:n.2957+66_2957+67insACA
NM_053002.6:c.2852+66_2852+67insACA (MED12L)	NP_443728.3:n.2852+66_2852+67insACA