Canonical Allele Identifier: CA354618047
Community Standard Title: NM_005630.3(SLCO2A1):c.614C>T (p.Pro205Leu)
Gene: SLCO2A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.133954977G>A , CM000665.2:g.133954977G>A GRCh38
NC_000003.11:g.133673821G>A , CM000665.1:g.133673821G>A GRCh37
NC_000003.10:g.135156511G>A NCBI36
NG_031964.2:g.102208C>T
NG_031964.3:g.102208C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005630.3:c.614C>T MANE Select NP_005621.2:p.Pro205Leu
ENST00000310926.11:c.614C>T MANE Select ENSP00000311291.4:p.Pro205Leu
NM_005630.2:c.614C>T NP_005621.2:p.Pro205Leu
ENST00000310926.8:c.614C>T ENSP00000311291.4:p.Pro205Leu
ENST00000462770.5:n.521-6277C>T
ENST00000464676.5:n.876C>T
ENST00000481359.3:c.614C>T ENSP00000420028.3:p.Pro205Leu
ENST00000493729.5:c.398-1216C>T ENSP00000418893.1:n.398-1216C>T
XM_011513090.1:c.614C>T XP_011511392.1:p.Pro205Leu
XM_017007077.1:c.110C>T XP_016862566.1:p.Pro37Leu
XM_024453721.1:c.614C>T XP_024309489.1:p.Pro205Leu