Canonical Allele Identifier: CA1583144456

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385176G= , CM000667.2:g.132385176G=	GRCh38
NC_000005.9:g.131720868G= , CM000667.1:g.131720868G=	GRCh37
NC_000005.8:g.131748767G=	NCBI36
NG_008982.1:g.20468G=
NG_008982.2:g.20473G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+862G=	ENSP00000388838.2:n.665+862G=
ENST00000435065.7:c.725-152G=	ENSP00000402760.2:n.725-152G=
ENST00000448810.6:c.653-152G=	ENSP00000401860.2:n.653-152G=
ENST00000686757.1:c.672-152G=	ENSP00000510721.1:n.672-152G=
ENST00000687740.1:n.1661G=
ENST00000688151.1:n.1845-152G=
ENST00000689271.1:c.671+856G=	ENSP00000510797.1:n.671+856G=
ENST00000690900.1:c.672-200G=	ENSP00000510703.1:n.672-200G=
ENST00000692212.1:n.327G=
ENST00000692355.1:c.204+875G=
ENST00000692413.1:c.672-152G=	ENSP00000509374.1:n.672-152G=
ENST00000692825.1:c.721-152G=	ENSP00000509447.1:n.721-152G=
ENST00000693308.1:c.666-152G=	ENSP00000509770.1:n.666-152G=
ENST00000693763.1:n.1661G=
ENST00000245407.8:c.653-152G= MANE Select	ENSP00000245407.3:n.653-152G=
ENST00000245407.7:c.653-152G=	ENSP00000245407.3:n.653-152G=
ENST00000415928.5:c.422-152G=	ENSP00000388838.1:n.422-152G=
ENST00000435065.6:c.725-152G=	ENSP00000402760.2:n.725-152G=
ENST00000437841.6:c.394-152G=	ENSP00000400553.1:n.394-152G=
ENST00000461013.5:n.8075-152G=
NM_001308122.1:c.725-152G=	NP_001295051.1:n.725-152G=
NM_003060.3:c.653-152G=	NP_003051.1:n.653-152G=
XM_011543590.1:c.35-152G=	XP_011541892.1:n.35-152G=
XR_427718.1:n.1013-152G=
XR_948290.1:n.994-152G=
XR_948291.1:n.1007-152G=
XM_011543590.2:c.35-152G=	XP_011541892.1:n.35-152G=
XM_017009778.2:c.125-152G=	XP_016865267.1:n.125-152G=
XR_001742215.1:n.994-152G=
XR_001742216.1:n.1013-152G=
XR_427718.2:n.1013-152G=
XR_948290.2:n.994-152G=
XR_948291.2:n.1007-152G=
NM_003060.4:c.653-152G= MANE Select	NP_003051.1:n.653-152G=
NM_001308122.2:c.725-152G=	NP_001295051.1:n.725-152G=