Canonical Allele Identifier: CA1583144544

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393761C= , CM000667.2:g.132393761C=	GRCh38
NC_000005.9:g.131729453C= , CM000667.1:g.131729453C=	GRCh37
NC_000005.8:g.131757352C=	NCBI36
NG_008982.1:g.29053C=
NG_008982.2:g.29058C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-424C=	ENSP00000388838.2:n.1292-424C=
ENST00000435065.7:c.1608C=	ENSP00000402760.2:p.Ser536=
ENST00000448810.6:c.*388C=	ENSP00000401860.2:n.*388C=
ENST00000685543.1:n.1677C=
ENST00000686757.1:c.*700C=	ENSP00000510721.1:n.*700C=
ENST00000686868.1:n.528C=
ENST00000687740.1:n.4221C=
ENST00000688151.1:n.2846C=
ENST00000689271.1:c.1383C=	ENSP00000510797.1:p.Ser461=
ENST00000690900.1:c.*700C=	ENSP00000510703.1:n.*700C=
ENST00000692212.1:n.4676C=
ENST00000692355.1:c.789C=
ENST00000692413.1:c.1518C=	ENSP00000509374.1:p.Ser506=
ENST00000692825.1:c.1604C=	ENSP00000509447.1:n.1604C=
ENST00000693308.1:c.1584C=	ENSP00000509770.1:p.Ser528=
ENST00000693763.1:n.2696C=
ENST00000245407.8:c.1536C= MANE Select	ENSP00000245407.3:p.Ser512=
ENST00000245407.7:c.1536C=	ENSP00000245407.3:p.Ser512=
ENST00000435065.6:c.1608C=	ENSP00000402760.2:p.Ser536=
ENST00000447841.5:c.380C=
ENST00000448810.5:c.798C=
ENST00000461013.5:n.8958C=
ENST00000475308.1:n.2214C=
NM_001308122.1:c.1608C=	NP_001295051.1:p.Ser536=
NM_003060.3:c.1536C=	NP_003051.1:p.Ser512=
XM_011543590.1:c.918C=	XP_011541892.1:p.Ser306=
XR_948290.1:n.1662C=
XM_011543590.2:c.918C=	XP_011541892.1:p.Ser306=
XM_017009778.2:c.1008C=	XP_016865267.1:p.Ser336=
XR_001742215.1:n.1791C=
XR_001742216.1:n.1810C=
XR_427718.2:n.1896C=
XR_948290.2:n.1662C=
XR_948291.2:n.1890C=
NM_003060.4:c.1536C= MANE Select	NP_003051.1:p.Ser512=
NM_001308122.2:c.1608C=	NP_001295051.1:p.Ser536=