Canonical Allele Identifier: CA1583144499
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393726C= , CM000667.2:g.132393726C= GRCh38
NC_000005.9:g.131729418C= , CM000667.1:g.131729418C= GRCh37
NC_000005.8:g.131757317C= NCBI36
NG_008982.1:g.29018C=
NG_008982.2:g.29023C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-459C= ENSP00000388838.2:n.1292-459C=
ENST00000435065.7:c.1573C= ENSP00000402760.2:p.Leu525=
ENST00000448810.6:c.*353C= ENSP00000401860.2:n.*353C=
ENST00000685543.1:n.1642C=
ENST00000686757.1:c.*665C= ENSP00000510721.1:n.*665C=
ENST00000686868.1:n.493C=
ENST00000687740.1:n.4186C=
ENST00000688151.1:n.2811C=
ENST00000689271.1:c.1348C= ENSP00000510797.1:p.Leu450=
ENST00000690900.1:c.*665C= ENSP00000510703.1:n.*665C=
ENST00000692212.1:n.4641C=
ENST00000692355.1:c.754C=
ENST00000692413.1:c.1483C= ENSP00000509374.1:p.Leu495=
ENST00000692825.1:c.1569C= ENSP00000509447.1:n.1569C=
ENST00000693308.1:c.1549C= ENSP00000509770.1:p.Leu517=
ENST00000693763.1:n.2661C=
ENST00000245407.8:c.1501C= MANE Select ENSP00000245407.3:p.Leu501=
ENST00000245407.7:c.1501C= ENSP00000245407.3:p.Leu501=
ENST00000435065.6:c.1573C= ENSP00000402760.2:p.Leu525=
ENST00000447841.5:c.345C=
ENST00000448810.5:c.763C=
ENST00000461013.5:n.8923C=
ENST00000475308.1:n.2179C=
NM_001308122.1:c.1573C= NP_001295051.1:p.Leu525=
NM_003060.3:c.1501C= NP_003051.1:p.Leu501=
XM_011543590.1:c.883C= XP_011541892.1:p.Leu295=
XR_948290.1:n.1627C=
XM_011543590.2:c.883C= XP_011541892.1:p.Leu295=
XM_017009778.2:c.973C= XP_016865267.1:p.Leu325=
XR_001742215.1:n.1756C=
XR_001742216.1:n.1775C=
XR_427718.2:n.1861C=
XR_948290.2:n.1627C=
XR_948291.2:n.1855C=
NM_003060.4:c.1501C= MANE Select NP_003051.1:p.Leu501=
NM_001308122.2:c.1573C= NP_001295051.1:p.Leu525=