Canonical Allele Identifier: CA1583144494
Gene: SLC22A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132393725C= , CM000667.2:g.132393725C= GRCh38
NC_000005.9:g.131729417C= , CM000667.1:g.131729417C= GRCh37
NC_000005.8:g.131757316C= NCBI36
NG_008982.1:g.29017C=
NG_008982.2:g.29022C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000415928.6:c.1292-460C= ENSP00000388838.2:n.1292-460C=
ENST00000435065.7:c.1572C= ENSP00000402760.2:p.Ile524=
ENST00000448810.6:c.*352C= ENSP00000401860.2:n.*352C=
ENST00000685543.1:n.1641C=
ENST00000686757.1:c.*664C= ENSP00000510721.1:n.*664C=
ENST00000686868.1:n.492C=
ENST00000687740.1:n.4185C=
ENST00000688151.1:n.2810C=
ENST00000689271.1:c.1347C= ENSP00000510797.1:p.Ile449=
ENST00000690900.1:c.*664C= ENSP00000510703.1:n.*664C=
ENST00000692212.1:n.4640C=
ENST00000692355.1:c.753C=
ENST00000692413.1:c.1482C= ENSP00000509374.1:p.Ile494=
ENST00000692825.1:c.1568C= ENSP00000509447.1:n.1568C=
ENST00000693308.1:c.1548C= ENSP00000509770.1:p.Ile516=
ENST00000693763.1:n.2660C=
ENST00000245407.8:c.1500C= MANE Select ENSP00000245407.3:p.Ile500=
ENST00000245407.7:c.1500C= ENSP00000245407.3:p.Ile500=
ENST00000435065.6:c.1572C= ENSP00000402760.2:p.Ile524=
ENST00000447841.5:c.344C=
ENST00000448810.5:c.762C=
ENST00000461013.5:n.8922C=
ENST00000475308.1:n.2178C=
NM_001308122.1:c.1572C= NP_001295051.1:p.Ile524=
NM_003060.3:c.1500C= NP_003051.1:p.Ile500=
XM_011543590.1:c.882C= XP_011541892.1:p.Ile294=
XR_948290.1:n.1626C=
XM_011543590.2:c.882C= XP_011541892.1:p.Ile294=
XM_017009778.2:c.972C= XP_016865267.1:p.Ile324=
XR_001742215.1:n.1755C=
XR_001742216.1:n.1774C=
XR_427718.2:n.1860C=
XR_948290.2:n.1626C=
XR_948291.2:n.1854C=
NM_003060.4:c.1500C= MANE Select NP_003051.1:p.Ile500=
NM_001308122.2:c.1572C= NP_001295051.1:p.Ile524=