Canonical Allele Identifier: CA354974389

Gene: MED12L P2RY12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151384142C>G , CM000665.2:g.151384142C>G	GRCh38
NC_000003.11:g.151101930C>G , CM000665.1:g.151101930C>G	GRCh37
NC_000003.10:g.152584620C>G	NCBI36
NG_016019.1:g.5615G>C , LRG_569:g.5615G>C
NG_021244.1:g.302255C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686666.1:c.4463C>G (MED12L)	ENSP00000509482.1:p.Ser1488Cys
ENST00000687756.1:c.4850C>G (MED12L) MANE Select	ENSP00000508695.1:p.Ser1617Cys
ENST00000302632.4:c.-180+550G>C (P2RY12) MANE Select	ENSP00000307259.4:n.-180+550G>C
ENST00000273432.8:c.4325C>G (MED12L)	ENSP00000273432.4:p.Ser1442Cys
ENST00000302632.3:c.-180+550G>C (P2RY12)	ENSP00000307259.3:n.-180+550G>C
ENST00000474524.5:c.4745C>G (MED12L)	ENSP00000417235.1:p.Ser1582Cys
NM_022788.4:c.-180+550G>C , LRG_569t1:c.-180+550G>C (P2RY12)	NP_073625.1:n.-180+550G>C
NM_053002.5:c.4745C>G (MED12L)	NP_443728.3:p.Ser1582Cys
XM_006713487.2:c.4850C>G (MED12L)	XP_006713550.1:p.Ser1617Cys
XM_011512386.1:c.4850C>G (MED12L)	XP_011510688.1:p.Ser1617Cys
XM_011512387.1:c.4847C>G (MED12L)	XP_011510689.1:p.Ser1616Cys
XM_011512388.1:c.4850C>G (MED12L)	XP_011510690.1:p.Ser1617Cys
XM_011512389.1:c.4745C>G (MED12L)	XP_011510691.1:p.Ser1582Cys
XM_011512390.1:c.4745C>G (MED12L)	XP_011510692.1:p.Ser1582Cys
XM_011512391.1:c.4580C>G (MED12L)	XP_011510693.1:p.Ser1527Cys
XM_011512392.1:c.4394C>G (MED12L)	XP_011510694.1:p.Ser1465Cys
XM_011512393.1:c.4850C>G (MED12L)	XP_011510695.1:p.Ser1617Cys
XM_011512394.1:c.4850C>G (MED12L)	XP_011510696.1:p.Ser1617Cys
XM_011512395.1:c.4850C>G (MED12L)	XP_011510697.1:p.Ser1617Cys
XM_011512396.1:c.3275C>G (MED12L)	XP_011510698.1:p.Ser1092Cys
XM_011512397.1:c.2717C>G (MED12L)	XP_011510699.1:p.Ser906Cys
XM_011512398.1:c.2645C>G (MED12L)	XP_011510700.1:p.Ser882Cys
XM_011512400.1:c.1667C>G (MED12L)	XP_011510702.1:p.Ser556Cys
XM_006713487.3:c.4850C>G (MED12L)	XP_006713550.1:p.Ser1617Cys
XM_011512390.2:c.4745C>G (MED12L)	XP_011510692.1:p.Ser1582Cys
XM_011512394.2:c.4850C>G (MED12L)	XP_011510696.1:p.Ser1617Cys
XM_017005676.1:c.4850C>G (MED12L)	XP_016861165.1:p.Ser1617Cys
XM_017005677.1:c.4847C>G (MED12L)	XP_016861166.1:p.Ser1616Cys
XM_017005678.1:c.4850C>G (MED12L)	XP_016861167.1:p.Ser1617Cys
XM_017005679.1:c.4580C>G (MED12L)	XP_016861168.1:p.Ser1527Cys
XM_017005680.1:c.4568C>G (MED12L)	XP_016861169.1:p.Ser1523Cys
XM_017005681.1:c.2237C>G (MED12L)	XP_016861170.1:p.Ser746Cys
XR_001740000.1:n.5247C>G (MED12L)
NM_022788.5:c.-180+550G>C (P2RY12) MANE Select	NP_073625.1:n.-180+550G>C
NM_001393769.1:c.4850C>G (MED12L) MANE Select	NP_001380698.1:p.Ser1617Cys
NM_053002.6:c.4745C>G (MED12L)	NP_443728.3:p.Ser1582Cys