Canonical Allele Identifier: CA2021001532

Gene: SLCO1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21200808_21200810delinsCAA , CM000674.2:g.21200808_21200810delinsCAA	GRCh38
NC_000012.11:g.21353742_21353744delinsCAA , CM000674.1:g.21353742_21353744delinsCAA	GRCh37
NC_000012.10:g.21245009_21245011delinsCAA	NCBI36
NG_011745.1:g.74615_74617delinsCAA , LRG_1022:g.74615_74617delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256958.3:c.1135+136_1135+138delinsCAA MANE Select	ENSP00000256958.2:n.1135+136_1135+138delinsCAA
ENST00000256958.2:c.1135+136_1135+138delinsCAA	ENSP00000256958.2:n.1135+136_1135+138delinsCAA
NM_006446.4:c.1135+136_1135+138delinsCAA , LRG_1022t1:c.1135+136_1135+138delinsCAA	NP_006437.3:n.1135+136_1135+138delinsCAA
NM_006446.5:c.1135+136_1135+138delinsCAA MANE Select	NP_006437.3:n.1135+136_1135+138delinsCAA