Canonical Allele Identifier: CA1583144518

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385282G= , CM000667.2:g.132385282G=	GRCh38
NC_000005.9:g.131720974G= , CM000667.1:g.131720974G=	GRCh37
NC_000005.8:g.131748873G=	NCBI36
NG_008982.1:g.20574G=
NG_008982.2:g.20579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+968G=	ENSP00000388838.2:n.665+968G=
ENST00000435065.7:c.725-46G=	ENSP00000402760.2:n.725-46G=
ENST00000448810.6:c.653-46G=	ENSP00000401860.2:n.653-46G=
ENST00000686757.1:c.672-46G=	ENSP00000510721.1:n.672-46G=
ENST00000687740.1:n.1767G=
ENST00000688151.1:n.1845-46G=
ENST00000689271.1:c.671+962G=	ENSP00000510797.1:n.671+962G=
ENST00000690900.1:c.672-94G=	ENSP00000510703.1:n.672-94G=
ENST00000692212.1:n.433G=
ENST00000692355.1:c.204+981G=
ENST00000692413.1:c.672-46G=	ENSP00000509374.1:n.672-46G=
ENST00000692825.1:c.721-46G=	ENSP00000509447.1:n.721-46G=
ENST00000693308.1:c.666-46G=	ENSP00000509770.1:n.666-46G=
ENST00000693763.1:n.1767G=
ENST00000245407.8:c.653-46G= MANE Select	ENSP00000245407.3:n.653-46G=
ENST00000245407.7:c.653-46G=	ENSP00000245407.3:n.653-46G=
ENST00000415928.5:c.422-46G=	ENSP00000388838.1:n.422-46G=
ENST00000435065.6:c.725-46G=	ENSP00000402760.2:n.725-46G=
ENST00000437841.6:c.394-46G=	ENSP00000400553.1:n.394-46G=
ENST00000461013.5:n.8075-46G=
NM_001308122.1:c.725-46G=	NP_001295051.1:n.725-46G=
NM_003060.3:c.653-46G=	NP_003051.1:n.653-46G=
XM_011543590.1:c.35-46G=	XP_011541892.1:n.35-46G=
XR_427718.1:n.1013-46G=
XR_948290.1:n.994-46G=
XR_948291.1:n.1007-46G=
XM_011543590.2:c.35-46G=	XP_011541892.1:n.35-46G=
XM_017009778.2:c.125-46G=	XP_016865267.1:n.125-46G=
XR_001742215.1:n.994-46G=
XR_001742216.1:n.1013-46G=
XR_427718.2:n.1013-46G=
XR_948290.2:n.994-46G=
XR_948291.2:n.1007-46G=
NM_003060.4:c.653-46G= MANE Select	NP_003051.1:n.653-46G=
NM_001308122.2:c.725-46G=	NP_001295051.1:n.725-46G=