Canonical Allele Identifier: CA16161939
Gene: MED12L HGNC NCBI
P2RY12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.151339854G>A , CM000665.2:g.151339854G>A GRCh38
NC_000003.11:g.151057642G>A , CM000665.1:g.151057642G>A GRCh37
NC_000003.10:g.152540332G>A NCBI36
NG_016019.1:g.49903C>T , LRG_569:g.49903C>T
NG_021244.1:g.257967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000685357.1:n.2509-10205G>A (MED12L)
ENST00000686666.1:c.1864-10205G>A (MED12L) ENSP00000509482.1:n.1864-10205G>A
ENST00000687756.1:c.2251-10205G>A (MED12L) MANE Select ENSP00000508695.1:n.2251-10205G>A
ENST00000693531.1:n.2326-10205G>A (MED12L)
ENST00000302632.4:c.-15+742C>T (P2RY12) MANE Select ENSP00000307259.4:n.-15+742C>T
ENST00000273432.8:c.1726-10205G>A (MED12L) ENSP00000273432.4:n.1726-10205G>A
ENST00000302632.3:c.-15+742C>T (P2RY12) ENSP00000307259.3:n.-15+742C>T
ENST00000468305.1:n.328-10205G>A (MED12L)
ENST00000468596.1:n.258+742C>T (P2RY12)
ENST00000474524.5:c.2146-10205G>A (MED12L) ENSP00000417235.1:n.2146-10205G>A
ENST00000491549.5:n.74-10205G>A (MED12L)
NM_022788.4:c.-15+742C>T , LRG_569t1:c.-15+742C>T (P2RY12) NP_073625.1:n.-15+742C>T
NM_053002.5:c.2146-10205G>A (MED12L) NP_443728.3:n.2146-10205G>A
NM_176876.2:c.-15+742C>T (P2RY12) NP_795345.1:n.-15+742C>T
XM_006713487.2:c.2251-10205G>A (MED12L) XP_006713550.1:n.2251-10205G>A
XM_011512386.1:c.2251-10205G>A (MED12L) XP_011510688.1:n.2251-10205G>A
XM_011512387.1:c.2251-10205G>A (MED12L) XP_011510689.1:n.2251-10205G>A
XM_011512388.1:c.2251-10205G>A (MED12L) XP_011510690.1:n.2251-10205G>A
XM_011512389.1:c.2146-10205G>A (MED12L) XP_011510691.1:n.2146-10205G>A
XM_011512390.1:c.2146-10205G>A (MED12L) XP_011510692.1:n.2146-10205G>A
XM_011512391.1:c.1981-10205G>A (MED12L) XP_011510693.1:n.1981-10205G>A
XM_011512392.1:c.1795-10205G>A (MED12L) XP_011510694.1:n.1795-10205G>A
XM_011512393.1:c.2251-10205G>A (MED12L) XP_011510695.1:n.2251-10205G>A
XM_011512394.1:c.2251-10205G>A (MED12L) XP_011510696.1:n.2251-10205G>A
XM_011512395.1:c.2251-10205G>A (MED12L) XP_011510697.1:n.2251-10205G>A
XM_011512396.1:c.676-10205G>A (MED12L) XP_011510698.1:n.676-10205G>A
XM_011512398.1:c.46-10205G>A (MED12L) XP_011510700.1:n.46-10205G>A
XM_011512399.1:c.2251-10205G>A (MED12L) XP_011510701.1:n.2251-10205G>A
XM_006713487.3:c.2251-10205G>A (MED12L) XP_006713550.1:n.2251-10205G>A
XM_011512390.2:c.2146-10205G>A (MED12L) XP_011510692.1:n.2146-10205G>A
XM_011512394.2:c.2251-10205G>A (MED12L) XP_011510696.1:n.2251-10205G>A
XM_011512399.3:c.2251-10205G>A (MED12L) XP_011510701.1:n.2251-10205G>A
XM_017005676.1:c.2251-10205G>A (MED12L) XP_016861165.1:n.2251-10205G>A
XM_017005677.1:c.2251-10205G>A (MED12L) XP_016861166.1:n.2251-10205G>A
XM_017005678.1:c.2251-10205G>A (MED12L) XP_016861167.1:n.2251-10205G>A
XM_017005679.1:c.1981-10205G>A (MED12L) XP_016861168.1:n.1981-10205G>A
XM_017005680.1:c.1969-10205G>A (MED12L) XP_016861169.1:n.1969-10205G>A
XR_001740000.1:n.2652-10205G>A (MED12L)
NM_022788.5:c.-15+742C>T (P2RY12) MANE Select NP_073625.1:n.-15+742C>T
NM_176876.3:c.-15+742C>T (P2RY12) NP_795345.1:n.-15+742C>T
NM_001393769.1:c.2251-10205G>A (MED12L) MANE Select NP_001380698.1:n.2251-10205G>A
NM_053002.6:c.2146-10205G>A (MED12L) NP_443728.3:n.2146-10205G>A
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