Canonical Allele Identifier: CA1583151824

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392497C= , CM000667.2:g.132392497C=	GRCh38
NC_000005.9:g.131728189C= , CM000667.1:g.131728189C=	GRCh37
NC_000005.8:g.131756088C=	NCBI36
NG_008982.1:g.27789C=
NG_008982.2:g.27794C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1173C=	ENSP00000388838.2:p.Ser391=
ENST00000435065.7:c.1404C=	ENSP00000402760.2:p.Ser468=
ENST00000448810.6:c.*184C=	ENSP00000401860.2:n.*184C=
ENST00000685543.1:n.1473C=
ENST00000686757.1:c.*496C=	ENSP00000510721.1:n.*496C=
ENST00000687740.1:n.4017C=
ENST00000688151.1:n.2642C=
ENST00000689271.1:c.1179C=	ENSP00000510797.1:p.Ser393=
ENST00000690900.1:c.*496C=	ENSP00000510703.1:n.*496C=
ENST00000692212.1:n.4472C=
ENST00000692355.1:c.585C=
ENST00000692413.1:c.1314C=	ENSP00000509374.1:p.Ser438=
ENST00000692825.1:c.1400C=	ENSP00000509447.1:n.1400C=
ENST00000693308.1:c.1380C=	ENSP00000509770.1:p.Ser460=
ENST00000693763.1:n.2492C=
ENST00000245407.8:c.1332C= MANE Select	ENSP00000245407.3:p.Ser444=
ENST00000245407.7:c.1332C=	ENSP00000245407.3:p.Ser444=
ENST00000435065.6:c.1404C=	ENSP00000402760.2:p.Ser468=
ENST00000447841.5:c.176C=
ENST00000448810.5:c.594C=
ENST00000461013.5:n.8754C=
ENST00000475308.1:n.2010C=
ENST00000479605.5:n.435C=
NM_001308122.1:c.1404C=	NP_001295051.1:p.Ser468=
NM_003060.3:c.1332C=	NP_003051.1:p.Ser444=
XM_011543590.1:c.714C=	XP_011541892.1:p.Ser238=
XR_948290.1:n.1458C=
XM_011543590.2:c.714C=	XP_011541892.1:p.Ser238=
XM_017009778.2:c.804C=	XP_016865267.1:p.Ser268=
XR_001742215.1:n.1587C=
XR_001742216.1:n.1606C=
XR_427718.2:n.1692C=
XR_948290.2:n.1458C=
XR_948291.2:n.1686C=
NM_003060.4:c.1332C= MANE Select	NP_003051.1:p.Ser444=
NM_001308122.2:c.1404C=	NP_001295051.1:p.Ser468=