Canonical Allele Identifier: CA1583146223

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387057C= , CM000667.2:g.132387057C=	GRCh38
NC_000005.9:g.131722749C= , CM000667.1:g.131722749C=	GRCh37
NC_000005.8:g.131750648C=	NCBI36
NG_008982.1:g.22349C=
NG_008982.2:g.22354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.698C=	ENSP00000388838.2:p.Ser233=
ENST00000435065.7:c.929C=	ENSP00000402760.2:p.Ser310=
ENST00000448810.6:c.857C=	ENSP00000401860.2:p.Ser286=
ENST00000686757.1:c.*21C=	ENSP00000510721.1:n.*21C=
ENST00000687740.1:n.3542C=
ENST00000688151.1:n.2167C=
ENST00000689271.1:c.704C=	ENSP00000510797.1:p.Ser235=
ENST00000690900.1:c.*21C=	ENSP00000510703.1:n.*21C=
ENST00000692212.1:n.801C=
ENST00000692355.1:c.205-1864C=
ENST00000692413.1:c.844-5C=	ENSP00000509374.1:n.844-5C=
ENST00000692825.1:c.925C=	ENSP00000509447.1:n.925C=
ENST00000693308.1:c.905C=	ENSP00000509770.1:p.Ser302=
ENST00000693763.1:n.2017C=
ENST00000245407.8:c.857C= MANE Select	ENSP00000245407.3:p.Ser286=
ENST00000245407.7:c.857C=	ENSP00000245407.3:p.Ser286=
ENST00000415928.5:c.626C=	ENSP00000388838.1:p.Ser209=
ENST00000435065.6:c.929C=	ENSP00000402760.2:p.Ser310=
ENST00000437841.6:c.*172C=	ENSP00000400553.1:n.*172C=
ENST00000448810.5:c.205C=
ENST00000461013.5:n.8279C=
NM_001308122.1:c.929C=	NP_001295051.1:p.Ser310=
NM_003060.3:c.857C=	NP_003051.1:p.Ser286=
XM_011543590.1:c.239C=	XP_011541892.1:p.Ser80=
XR_427718.1:n.1217C=
XR_948290.1:n.1198C=
XR_948291.1:n.1211C=
XM_011543590.2:c.239C=	XP_011541892.1:p.Ser80=
XM_017009778.2:c.329C=	XP_016865267.1:p.Ser110=
XR_001742215.1:n.1198C=
XR_001742216.1:n.1217C=
XR_427718.2:n.1217C=
XR_948290.2:n.1198C=
XR_948291.2:n.1211C=
NM_003060.4:c.857C= MANE Select	NP_003051.1:p.Ser286=
NM_001308122.2:c.929C=	NP_001295051.1:p.Ser310=