Canonical Allele Identifier: CA1583144506

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393730C= , CM000667.2:g.132393730C=	GRCh38
NC_000005.9:g.131729422C= , CM000667.1:g.131729422C=	GRCh37
NC_000005.8:g.131757321C=	NCBI36
NG_008982.1:g.29022C=
NG_008982.2:g.29027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-455C=	ENSP00000388838.2:n.1292-455C=
ENST00000435065.7:c.1577C=	ENSP00000402760.2:p.Thr526=
ENST00000448810.6:c.*357C=	ENSP00000401860.2:n.*357C=
ENST00000685543.1:n.1646C=
ENST00000686757.1:c.*669C=	ENSP00000510721.1:n.*669C=
ENST00000686868.1:n.497C=
ENST00000687740.1:n.4190C=
ENST00000688151.1:n.2815C=
ENST00000689271.1:c.1352C=	ENSP00000510797.1:p.Thr451=
ENST00000690900.1:c.*669C=	ENSP00000510703.1:n.*669C=
ENST00000692212.1:n.4645C=
ENST00000692355.1:c.758C=
ENST00000692413.1:c.1487C=	ENSP00000509374.1:p.Thr496=
ENST00000692825.1:c.1573C=	ENSP00000509447.1:n.1573C=
ENST00000693308.1:c.1553C=	ENSP00000509770.1:p.Thr518=
ENST00000693763.1:n.2665C=
ENST00000245407.8:c.1505C= MANE Select	ENSP00000245407.3:p.Thr502=
ENST00000245407.7:c.1505C=	ENSP00000245407.3:p.Thr502=
ENST00000435065.6:c.1577C=	ENSP00000402760.2:p.Thr526=
ENST00000447841.5:c.349C=
ENST00000448810.5:c.767C=
ENST00000461013.5:n.8927C=
ENST00000475308.1:n.2183C=
NM_001308122.1:c.1577C=	NP_001295051.1:p.Thr526=
NM_003060.3:c.1505C=	NP_003051.1:p.Thr502=
XM_011543590.1:c.887C=	XP_011541892.1:p.Thr296=
XR_948290.1:n.1631C=
XM_011543590.2:c.887C=	XP_011541892.1:p.Thr296=
XM_017009778.2:c.977C=	XP_016865267.1:p.Thr326=
XR_001742215.1:n.1760C=
XR_001742216.1:n.1779C=
XR_427718.2:n.1865C=
XR_948290.2:n.1631C=
XR_948291.2:n.1859C=
NM_003060.4:c.1505C= MANE Select	NP_003051.1:p.Thr502=
NM_001308122.2:c.1577C=	NP_001295051.1:p.Thr526=