Canonical Allele Identifier: CA1583151810

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392490C= , CM000667.2:g.132392490C=	GRCh38
NC_000005.9:g.131728182C= , CM000667.1:g.131728182C=	GRCh37
NC_000005.8:g.131756081C=	NCBI36
NG_008982.1:g.27782C=
NG_008982.2:g.27787C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1166C=	ENSP00000388838.2:p.Ala389=
ENST00000435065.7:c.1397C=	ENSP00000402760.2:p.Ala466=
ENST00000448810.6:c.*177C=	ENSP00000401860.2:n.*177C=
ENST00000685543.1:n.1466C=
ENST00000686757.1:c.*489C=	ENSP00000510721.1:n.*489C=
ENST00000687740.1:n.4010C=
ENST00000688151.1:n.2635C=
ENST00000689271.1:c.1172C=	ENSP00000510797.1:p.Ala391=
ENST00000690900.1:c.*489C=	ENSP00000510703.1:n.*489C=
ENST00000692212.1:n.4465C=
ENST00000692355.1:c.578C=
ENST00000692413.1:c.1307C=	ENSP00000509374.1:p.Ala436=
ENST00000692825.1:c.1393C=	ENSP00000509447.1:n.1393C=
ENST00000693308.1:c.1373C=	ENSP00000509770.1:p.Ala458=
ENST00000693763.1:n.2485C=
ENST00000245407.8:c.1325C= MANE Select	ENSP00000245407.3:p.Ala442=
ENST00000245407.7:c.1325C=	ENSP00000245407.3:p.Ala442=
ENST00000435065.6:c.1397C=	ENSP00000402760.2:p.Ala466=
ENST00000447841.5:c.169C=
ENST00000448810.5:c.587C=
ENST00000461013.5:n.8747C=
ENST00000475308.1:n.2003C=
ENST00000479605.5:n.428C=
NM_001308122.1:c.1397C=	NP_001295051.1:p.Ala466=
NM_003060.3:c.1325C=	NP_003051.1:p.Ala442=
XM_011543590.1:c.707C=	XP_011541892.1:p.Ala236=
XR_948290.1:n.1451C=
XM_011543590.2:c.707C=	XP_011541892.1:p.Ala236=
XM_017009778.2:c.797C=	XP_016865267.1:p.Ala266=
XR_001742215.1:n.1580C=
XR_001742216.1:n.1599C=
XR_427718.2:n.1685C=
XR_948290.2:n.1451C=
XR_948291.2:n.1679C=
NM_003060.4:c.1325C= MANE Select	NP_003051.1:p.Ala442=
NM_001308122.2:c.1397C=	NP_001295051.1:p.Ala466=