Canonical Allele Identifier: CA1583144476
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393708A= , CM000667.2:g.132393708A= GRCh38
NC_000005.9:g.131729400A= , CM000667.1:g.131729400A= GRCh37
NC_000005.8:g.131757299A= NCBI36
NG_008982.1:g.29000A=
NG_008982.2:g.29005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-477A= ENSP00000388838.2:n.1292-477A=
ENST00000435065.7:c.1555A= ENSP00000402760.2:p.Met519=
ENST00000448810.6:c.*335A= ENSP00000401860.2:n.*335A=
ENST00000685543.1:n.1624A=
ENST00000686757.1:c.*647A= ENSP00000510721.1:n.*647A=
ENST00000686868.1:n.475A=
ENST00000687740.1:n.4168A=
ENST00000688151.1:n.2793A=
ENST00000689271.1:c.1330A= ENSP00000510797.1:p.Met444=
ENST00000690900.1:c.*647A= ENSP00000510703.1:n.*647A=
ENST00000692212.1:n.4623A=
ENST00000692355.1:c.736A=
ENST00000692413.1:c.1465A= ENSP00000509374.1:p.Met489=
ENST00000692825.1:c.1551A= ENSP00000509447.1:n.1551A=
ENST00000693308.1:c.1531A= ENSP00000509770.1:p.Met511=
ENST00000693763.1:n.2643A=
ENST00000245407.8:c.1483A= MANE Select ENSP00000245407.3:p.Met495=
ENST00000245407.7:c.1483A= ENSP00000245407.3:p.Met495=
ENST00000435065.6:c.1555A= ENSP00000402760.2:p.Met519=
ENST00000447841.5:c.327A=
ENST00000448810.5:c.745A=
ENST00000461013.5:n.8905A=
ENST00000475308.1:n.2161A=
NM_001308122.1:c.1555A= NP_001295051.1:p.Met519=
NM_003060.3:c.1483A= NP_003051.1:p.Met495=
XM_011543590.1:c.865A= XP_011541892.1:p.Met289=
XR_948290.1:n.1609A=
XM_011543590.2:c.865A= XP_011541892.1:p.Met289=
XM_017009778.2:c.955A= XP_016865267.1:p.Met319=
XR_001742215.1:n.1738A=
XR_001742216.1:n.1757A=
XR_427718.2:n.1843A=
XR_948290.2:n.1609A=
XR_948291.2:n.1837A=
NM_003060.4:c.1483A= MANE Select NP_003051.1:p.Met495=
NM_001308122.2:c.1555A= NP_001295051.1:p.Met519=