Canonical Allele Identifier: CA1583144721

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132394049G= , CM000667.2:g.132394049G=	GRCh38
NC_000005.9:g.131729741G= , CM000667.1:g.131729741G=	GRCh37
NC_000005.8:g.131757640G=	NCBI36
NG_008982.1:g.29341G=
NG_008982.2:g.29346G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1292-136G=	ENSP00000388838.2:n.1292-136G=
ENST00000435065.7:c.1659-136G=	ENSP00000402760.2:n.1659-136G=
ENST00000448810.6:c.*439-136G=	ENSP00000401860.2:n.*439-136G=
ENST00000685543.1:n.1728-136G=
ENST00000686757.1:c.*751-136G=	ENSP00000510721.1:n.*751-136G=
ENST00000686868.1:n.579-136G=
ENST00000687740.1:n.4272-136G=
ENST00000688151.1:n.2897-136G=
ENST00000689271.1:c.1434-136G=	ENSP00000510797.1:n.1434-136G=
ENST00000690900.1:c.*751-136G=	ENSP00000510703.1:n.*751-136G=
ENST00000692212.1:n.4727-136G=
ENST00000692355.1:c.840-136G=
ENST00000692413.1:c.1569-136G=	ENSP00000509374.1:n.1569-136G=
ENST00000692825.1:c.1655-136G=	ENSP00000509447.1:n.1655-136G=
ENST00000693308.1:c.1635-136G=	ENSP00000509770.1:n.1635-136G=
ENST00000693763.1:n.2747-136G=
ENST00000245407.8:c.1587-136G= MANE Select	ENSP00000245407.3:n.1587-136G=
ENST00000245407.7:c.1587-136G=	ENSP00000245407.3:n.1587-136G=
ENST00000435065.6:c.1659-136G=	ENSP00000402760.2:n.1659-136G=
ENST00000447841.5:c.431-136G=
ENST00000461013.5:n.9009-136G=
ENST00000475308.1:n.2265-136G=
NM_001308122.1:c.1659-136G=	NP_001295051.1:n.1659-136G=
NM_003060.3:c.1587-136G=	NP_003051.1:n.1587-136G=
XM_011543590.1:c.969-136G=	XP_011541892.1:n.969-136G=
XR_948290.1:n.1713-136G=
XM_011543590.2:c.969-136G=	XP_011541892.1:n.969-136G=
XM_017009778.2:c.1059-136G=	XP_016865267.1:n.1059-136G=
XR_001742215.1:n.1842-136G=
XR_001742216.1:n.1861-136G=
XR_427718.2:n.1947-136G=
XR_948290.2:n.1713-136G=
XR_948291.2:n.1941-136G=
NM_003060.4:c.1587-136G= MANE Select	NP_003051.1:n.1587-136G=
NM_001308122.2:c.1659-136G=	NP_001295051.1:n.1659-136G=