Canonical Allele Identifier: CA2021050479

Gene: SLCO1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21304514G= , CM000674.2:g.21304514G=	GRCh38
NC_000012.11:g.21457448G= , CM000674.1:g.21457448G=	GRCh37
NC_000012.10:g.21348715G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001386879.1:c.502C= MANE Select	NP_001373808.1:p.Arg168=
ENST00000683939.1:c.502C= MANE Select	ENSP00000508235.1:p.Arg168=
NM_001386878.1:c.502C=	NP_001373807.1:p.Arg168=
NM_001386880.1:c.502C=	NP_001373809.1:p.Arg168=
NM_001386881.1:c.502C=	NP_001373810.1:p.Arg168=
NM_001386882.1:c.502C=	NP_001373811.1:p.Arg168=
NM_001386882.2:c.502C=	NP_001373811.1:p.Arg168=
NM_001386886.1:c.496C=	NP_001373815.1:p.Arg166=
NM_001386887.1:c.502C=	NP_001373816.1:p.Arg168=
NM_001386890.1:c.34C=	NP_001373819.1:p.Arg12=
NM_001386908.1:c.241C=	NP_001373837.1:p.Arg81=
NM_001386919.1:c.241C=	NP_001373848.1:p.Arg81=
NM_001386920.1:c.34C=	NP_001373849.1:p.Arg12=
NM_001386921.1:c.202C=	NP_001373850.1:p.Arg68=
NM_001386922.1:c.106C=	NP_001373851.1:p.Arg36=
NM_001386926.1:c.496C=	NP_001373855.1:p.Arg166=
NM_001386927.1:c.241C=	NP_001373856.1:p.Arg81=
NM_001386929.1:c.106C=	NP_001373858.1:p.Arg36=
NM_001386931.1:c.34C=	NP_001373860.1:p.Arg12=
NM_001386937.1:c.106C=	NP_001373866.1:p.Arg36=
NM_001386938.1:c.106C=	NP_001373867.1:p.Arg36=
NM_001386939.1:c.106C=	NP_001373868.1:p.Arg36=
NM_001386940.1:c.106C=	NP_001373869.1:p.Arg36=
NM_001386946.1:c.442C=	NP_001373875.1:p.Arg148=
NM_001386947.1:c.496C=	NP_001373876.1:p.Arg166=
NM_001386948.1:c.442C=	NP_001373877.1:p.Arg148=
NM_001386949.1:c.496C=	NP_001373878.1:p.Arg166=
NM_001386951.1:c.442C=	NP_001373880.1:p.Arg148=
NM_001386952.1:c.442C=	NP_001373881.1:p.Arg148=
NM_001386953.1:c.34C=	NP_001373882.1:p.Arg12=
NM_001386954.1:c.34C=	NP_001373883.1:p.Arg12=
NM_001386958.1:c.442C=	NP_001373887.1:p.Arg148=
NM_001386959.1:c.442C=	NP_001373888.1:p.Arg148=
NM_001386960.1:c.496C=	NP_001373889.1:p.Arg166=
NM_001386961.1:c.34C=	NP_001373890.1:p.Arg12=
NM_001386962.1:c.106C=	NP_001373891.1:p.Arg36=
NM_001386963.1:c.241C=	NP_001373892.1:p.Arg81=
NM_021094.3:c.502C=	NP_066580.1:p.Arg168=
NM_021094.4:c.502C=	NP_066580.1:p.Arg168=
NM_134431.3:c.502C=	NP_602307.1:p.Arg168=
NM_134431.5:c.502C=	NP_602307.1:p.Arg168=
NR_170340.1:n.608C=
NR_170341.1:n.501C=
NR_170343.1:n.608C=
ENST00000307378.10:c.502C=	ENSP00000305974.6:p.Arg168=
ENST00000458504.5:c.106C=	ENSP00000394854.1:p.Arg36=
ENST00000463718.5:n.793C=
ENST00000480394.5:n.530C=
ENST00000544020.5:c.*81C=	ENSP00000440154.1:n.*81C=
ENST00000544290.5:c.*81C=	ENSP00000438348.1:n.*81C=
XM_005253474.3:c.502C=	XP_005253531.1:p.Arg168=
XM_005253477.2:c.442C=	XP_005253534.1:p.Arg148=
XM_005253477.3:c.442C=	XP_005253534.1:p.Arg148=
XM_011520818.1:c.502C=	XP_011519120.1:p.Arg168=
XM_011520819.1:c.502C=	XP_011519121.1:p.Arg168=
XM_011520820.1:c.496C=	XP_011519122.1:p.Arg166=
XM_011520820.3:c.496C=	XP_011519122.1:p.Arg166=
XM_017019849.1:c.502C=	XP_016875338.1:p.Arg168=
XM_017019850.1:c.442C=	XP_016875339.1:p.Arg148=
XM_024449138.1:c.502C=	XP_024304906.1:p.Arg168=
XM_024449139.1:c.502C=	XP_024304907.1:p.Arg168=