Canonical Allele Identifier: CA2667890

Gene: MED12L P2RY12

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.151338589T>C , CM000665.2:g.151338589T>C	GRCh38
NC_000003.11:g.151056377T>C , CM000665.1:g.151056377T>C	GRCh37
NC_000003.10:g.152539067T>C	NCBI36
NG_016019.1:g.51168A>G , LRG_569:g.51168A>G
NG_021244.1:g.256702T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685357.1:n.2509-11470T>C (MED12L)
ENST00000686666.1:c.1864-11470T>C (MED12L)	ENSP00000509482.1:n.1864-11470T>C
ENST00000687756.1:c.2251-11470T>C (MED12L) MANE Select	ENSP00000508695.1:n.2251-11470T>C
ENST00000693531.1:n.2326-11470T>C (MED12L)
ENST00000302632.4:c.257A>G (P2RY12) MANE Select	ENSP00000307259.4:p.Lys86Arg
ENST00000273432.8:c.1726-11470T>C (MED12L)	ENSP00000273432.4:n.1726-11470T>C
ENST00000302632.3:c.257A>G (P2RY12)	ENSP00000307259.3:p.Lys86Arg
ENST00000468305.1:n.328-11470T>C (MED12L)
ENST00000468596.1:n.529A>G (P2RY12)
ENST00000474524.5:c.2146-11470T>C (MED12L)	ENSP00000417235.1:n.2146-11470T>C
ENST00000491549.5:n.74-11470T>C (MED12L)
NM_022788.4:c.257A>G , LRG_569t1:c.257A>G (P2RY12)	NP_073625.1:p.Lys86Arg
NM_053002.5:c.2146-11470T>C (MED12L)	NP_443728.3:n.2146-11470T>C
NM_176876.2:c.257A>G (P2RY12)	NP_795345.1:p.Lys86Arg
XM_006713487.2:c.2251-11470T>C (MED12L)	XP_006713550.1:n.2251-11470T>C
XM_011512386.1:c.2251-11470T>C (MED12L)	XP_011510688.1:n.2251-11470T>C
XM_011512387.1:c.2251-11470T>C (MED12L)	XP_011510689.1:n.2251-11470T>C
XM_011512388.1:c.2251-11470T>C (MED12L)	XP_011510690.1:n.2251-11470T>C
XM_011512389.1:c.2146-11470T>C (MED12L)	XP_011510691.1:n.2146-11470T>C
XM_011512390.1:c.2146-11470T>C (MED12L)	XP_011510692.1:n.2146-11470T>C
XM_011512391.1:c.1981-11470T>C (MED12L)	XP_011510693.1:n.1981-11470T>C
XM_011512392.1:c.1795-11470T>C (MED12L)	XP_011510694.1:n.1795-11470T>C
XM_011512393.1:c.2251-11470T>C (MED12L)	XP_011510695.1:n.2251-11470T>C
XM_011512394.1:c.2251-11470T>C (MED12L)	XP_011510696.1:n.2251-11470T>C
XM_011512395.1:c.2251-11470T>C (MED12L)	XP_011510697.1:n.2251-11470T>C
XM_011512396.1:c.676-11470T>C (MED12L)	XP_011510698.1:n.676-11470T>C
XM_011512398.1:c.46-11470T>C (MED12L)	XP_011510700.1:n.46-11470T>C
XM_011512399.1:c.2251-11470T>C (MED12L)	XP_011510701.1:n.2251-11470T>C
XM_006713487.3:c.2251-11470T>C (MED12L)	XP_006713550.1:n.2251-11470T>C
XM_011512390.2:c.2146-11470T>C (MED12L)	XP_011510692.1:n.2146-11470T>C
XM_011512394.2:c.2251-11470T>C (MED12L)	XP_011510696.1:n.2251-11470T>C
XM_011512399.3:c.2251-11470T>C (MED12L)	XP_011510701.1:n.2251-11470T>C
XM_017005676.1:c.2251-11470T>C (MED12L)	XP_016861165.1:n.2251-11470T>C
XM_017005677.1:c.2251-11470T>C (MED12L)	XP_016861166.1:n.2251-11470T>C
XM_017005678.1:c.2251-11470T>C (MED12L)	XP_016861167.1:n.2251-11470T>C
XM_017005679.1:c.1981-11470T>C (MED12L)	XP_016861168.1:n.1981-11470T>C
XM_017005680.1:c.1969-11470T>C (MED12L)	XP_016861169.1:n.1969-11470T>C
XR_001740000.1:n.2652-11470T>C (MED12L)
NM_022788.5:c.257A>G (P2RY12) MANE Select	NP_073625.1:p.Lys86Arg
NM_176876.3:c.257A>G (P2RY12)	NP_795345.1:p.Lys86Arg
NM_001393769.1:c.2251-11470T>C (MED12L) MANE Select	NP_001380698.1:n.2251-11470T>C
NM_053002.6:c.2146-11470T>C (MED12L)	NP_443728.3:n.2146-11470T>C