Canonical Allele Identifier: CA360573839
Gene: SLCO6A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.102390990T>C , CM000667.2:g.102390990T>C GRCh38
NC_000005.9:g.101726694T>C , CM000667.1:g.101726694T>C GRCh37
NC_000005.8:g.101754593T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000506729.6:c.1870A>G MANE Select ENSP00000421339.1:p.Arg624Gly
ENST00000379807.7:c.1870A>G ENSP00000369135.3:p.Arg624Gly
ENST00000389019.7:c.1684A>G ENSP00000373671.3:p.Arg562Gly
ENST00000506729.5:c.1870A>G ENSP00000421339.1:p.Arg624Gly
ENST00000513675.1:c.1111A>G ENSP00000421990.1:p.Arg371Gly
ENST00000514765.6:n.240A>G
NM_001289002.1:c.1870A>G NP_001275931.1:p.Arg624Gly
NM_001289004.1:c.1684A>G NP_001275933.1:p.Arg562Gly
NM_001308014.1:c.1111A>G NP_001294943.1:p.Arg371Gly
NM_173488.4:c.1870A>G NP_775759.3:p.Arg624Gly
XM_005271874.2:c.1870A>G XP_005271931.1:p.Arg624Gly
XM_011543147.1:c.1765A>G XP_011541449.1:p.Arg589Gly
XM_011543148.1:c.1633A>G XP_011541450.1:p.Arg545Gly
XM_011543149.1:c.1297A>G XP_011541451.1:p.Arg433Gly
XM_011543150.1:c.1141A>G XP_011541452.1:p.Arg381Gly
XM_011543151.1:c.1111A>G XP_011541453.1:p.Arg371Gly
XM_011543153.1:c.1048A>G XP_011541455.1:p.Arg350Gly
XM_005271874.3:c.1870A>G XP_005271931.1:p.Arg624Gly
XM_011543147.2:c.1765A>G XP_011541449.1:p.Arg589Gly
XM_011543148.2:c.1633A>G XP_011541450.1:p.Arg545Gly
XM_011543153.2:c.1048A>G XP_011541455.1:p.Arg350Gly
NM_001289002.2:c.1870A>G NP_001275931.1:p.Arg624Gly
NM_001289004.2:c.1684A>G NP_001275933.1:p.Arg562Gly
NM_001308014.2:c.1111A>G NP_001294943.1:p.Arg371Gly
NM_173488.5:c.1870A>G MANE Select NP_775759.3:p.Arg624Gly