Canonical Allele Identifier: CA1583149814
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132390687C= , CM000667.2:g.132390687C= GRCh38
NC_000005.9:g.131726379C= , CM000667.1:g.131726379C= GRCh37
NC_000005.8:g.131754278C= NCBI36
NG_008982.1:g.25979C=
NG_008982.2:g.25984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.894-3C= ENSP00000388838.2:n.894-3C=
ENST00000435065.7:c.1125-3C= ENSP00000402760.2:n.1125-3C=
ENST00000448810.6:c.1053-89C= ENSP00000401860.2:n.1053-89C=
ENST00000685543.1:n.1194-3C=
ENST00000686757.1:c.*217-3C= ENSP00000510721.1:n.*217-3C=
ENST00000687740.1:n.3738-3C=
ENST00000688151.1:n.2363-3C=
ENST00000689271.1:c.900-3C= ENSP00000510797.1:n.900-3C=
ENST00000690900.1:c.*217-3C= ENSP00000510703.1:n.*217-3C=
ENST00000692212.1:n.2662C=
ENST00000692355.1:c.306-3C=
ENST00000692413.1:c.1035-3C= ENSP00000509374.1:n.1035-3C=
ENST00000692825.1:c.1121-3C= ENSP00000509447.1:n.1121-3C=
ENST00000693308.1:c.1101-3C= ENSP00000509770.1:n.1101-3C=
ENST00000693763.1:n.2213-3C=
ENST00000245407.8:c.1053-3C= MANE Select ENSP00000245407.3:n.1053-3C=
ENST00000245407.7:c.1053-3C= ENSP00000245407.3:n.1053-3C=
ENST00000435065.6:c.1125-3C= ENSP00000402760.2:n.1125-3C=
ENST00000447841.5:c.111+1666C=
ENST00000448810.5:c.401-89C=
ENST00000461013.5:n.8475-3C=
ENST00000475308.1:n.1728C=
ENST00000479605.5:n.156-3C=
NM_001308122.1:c.1125-3C= NP_001295051.1:n.1125-3C=
NM_003060.3:c.1053-3C= NP_003051.1:n.1053-3C=
XM_011543590.1:c.435-3C= XP_011541892.1:n.435-3C=
XR_427718.1:n.1413-3C=
XR_948290.1:n.1393+1666C=
XR_948291.1:n.1407-3C=
XM_011543590.2:c.435-3C= XP_011541892.1:n.435-3C=
XM_017009778.2:c.525-3C= XP_016865267.1:n.525-3C=
XR_001742215.1:n.1394-89C=
XR_001742216.1:n.1413-89C=
XR_427718.2:n.1413-3C=
XR_948290.2:n.1393+1666C=
XR_948291.2:n.1407-3C=
NM_003060.4:c.1053-3C= MANE Select NP_003051.1:n.1053-3C=
NM_001308122.2:c.1125-3C= NP_001295051.1:n.1125-3C=