Canonical Allele Identifier: CA2626497
Community Standard Title: NM_005630.3(SLCO2A1):c.1333C>T (p.Arg445Cys)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133945223G>A , CM000665.2:g.133945223G>A GRCh38
NC_000003.11:g.133664067G>A , CM000665.1:g.133664067G>A GRCh37
NC_000003.10:g.135146757G>A NCBI36
NG_031964.2:g.111962C>T
NG_031964.3:g.111962C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.1333C>T MANE Select NP_005621.2:p.Arg445Cys
ENST00000310926.11:c.1333C>T MANE Select ENSP00000311291.4:p.Arg445Cys
NM_005630.2:c.1333C>T NP_005621.2:p.Arg445Cys
ENST00000310926.8:c.1333C>T ENSP00000311291.4:p.Arg445Cys
ENST00000462770.5:n.913C>T
ENST00000481359.3:c.1143C>T ENSP00000420028.3:p.Ala381=
ENST00000493729.5:c.1105C>T ENSP00000418893.1:p.Arg369Cys
XM_011513090.1:c.1333C>T XP_011511392.1:p.Arg445Cys
XM_017007077.1:c.829C>T XP_016862566.1:p.Arg277Cys
XM_024453721.1:c.1333C>T XP_024309489.1:p.Arg445Cys