Canonical Allele Identifier: CA2668624
Gene: MED12L HGNC NCBI
P2RY12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1251486
dbSNP Id: rs10935841

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.151383903C>T , CM000665.2:g.151383903C>T GRCh38
NC_000003.11:g.151101691C>T , CM000665.1:g.151101691C>T GRCh37
NC_000003.10:g.152584381C>T NCBI36
NG_016019.1:g.5854G>A , LRG_569:g.5854G>A
NG_021244.1:g.302016C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000686666.1:c.4403+15C>T (MED12L) ENSP00000509482.1:n.4403+15C>T
ENST00000687756.1:c.4790+15C>T (MED12L) MANE Select ENSP00000508695.1:n.4790+15C>T
ENST00000302632.4:c.-180+789G>A (P2RY12) MANE Select ENSP00000307259.4:n.-180+789G>A
ENST00000273432.8:c.4265+15C>T (MED12L) ENSP00000273432.4:n.4265+15C>T
ENST00000302632.3:c.-180+789G>A (P2RY12) ENSP00000307259.3:n.-180+789G>A
ENST00000474524.5:c.4685+15C>T (MED12L) ENSP00000417235.1:n.4685+15C>T
NM_022788.4:c.-180+789G>A , LRG_569t1:c.-180+789G>A (P2RY12) NP_073625.1:n.-180+789G>A
NM_053002.5:c.4685+15C>T (MED12L) NP_443728.3:n.4685+15C>T
XM_006713487.2:c.4790+15C>T (MED12L) XP_006713550.1:n.4790+15C>T
XM_011512386.1:c.4790+15C>T (MED12L) XP_011510688.1:n.4790+15C>T
XM_011512387.1:c.4787+15C>T (MED12L) XP_011510689.1:n.4787+15C>T
XM_011512388.1:c.4790+15C>T (MED12L) XP_011510690.1:n.4790+15C>T
XM_011512389.1:c.4685+15C>T (MED12L) XP_011510691.1:n.4685+15C>T
XM_011512390.1:c.4685+15C>T (MED12L) XP_011510692.1:n.4685+15C>T
XM_011512391.1:c.4520+15C>T (MED12L) XP_011510693.1:n.4520+15C>T
XM_011512392.1:c.4334+15C>T (MED12L) XP_011510694.1:n.4334+15C>T
XM_011512393.1:c.4790+15C>T (MED12L) XP_011510695.1:n.4790+15C>T
XM_011512394.1:c.4790+15C>T (MED12L) XP_011510696.1:n.4790+15C>T
XM_011512395.1:c.4790+15C>T (MED12L) XP_011510697.1:n.4790+15C>T
XM_011512396.1:c.3215+15C>T (MED12L) XP_011510698.1:n.3215+15C>T
XM_011512397.1:c.2657+15C>T (MED12L) XP_011510699.1:n.2657+15C>T
XM_011512398.1:c.2585+15C>T (MED12L) XP_011510700.1:n.2585+15C>T
XM_011512400.1:c.1607+15C>T (MED12L) XP_011510702.1:n.1607+15C>T
XM_006713487.3:c.4790+15C>T (MED12L) XP_006713550.1:n.4790+15C>T
XM_011512390.2:c.4685+15C>T (MED12L) XP_011510692.1:n.4685+15C>T
XM_011512394.2:c.4790+15C>T (MED12L) XP_011510696.1:n.4790+15C>T
XM_017005676.1:c.4790+15C>T (MED12L) XP_016861165.1:n.4790+15C>T
XM_017005677.1:c.4787+15C>T (MED12L) XP_016861166.1:n.4787+15C>T
XM_017005678.1:c.4790+15C>T (MED12L) XP_016861167.1:n.4790+15C>T
XM_017005679.1:c.4520+15C>T (MED12L) XP_016861168.1:n.4520+15C>T
XM_017005680.1:c.4508+15C>T (MED12L) XP_016861169.1:n.4508+15C>T
XM_017005681.1:c.2177+15C>T (MED12L) XP_016861170.1:n.2177+15C>T
XR_001740000.1:n.5187+15C>T (MED12L)
NM_022788.5:c.-180+789G>A (P2RY12) MANE Select NP_073625.1:n.-180+789G>A
NM_001393769.1:c.4790+15C>T (MED12L) MANE Select NP_001380698.1:n.4790+15C>T
NM_053002.6:c.4685+15C>T (MED12L) NP_443728.3:n.4685+15C>T