Canonical Allele Identifier: CA1583141359

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132378486G= , CM000667.2:g.132378486G=	GRCh38
NC_000005.9:g.131714178G= , CM000667.1:g.131714178G=	GRCh37
NC_000005.8:g.131742077G=	NCBI36
NG_008982.1:g.13778G=
NG_008982.2:g.13783G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.497+5G=	ENSP00000388838.2:n.497+5G=
ENST00000435065.7:c.569+5G=	ENSP00000402760.2:n.569+5G=
ENST00000448810.6:c.497+5G=	ENSP00000401860.2:n.497+5G=
ENST00000686757.1:c.497+5G=	ENSP00000510721.1:n.497+5G=
ENST00000687740.1:n.631+5G=
ENST00000689271.1:c.497+5G=	ENSP00000510797.1:n.497+5G=
ENST00000690900.1:c.497+5G=	ENSP00000510703.1:n.497+5G=
ENST00000692355.1:c.49+5G=
ENST00000692413.1:c.497+5G=	ENSP00000509374.1:n.497+5G=
ENST00000692825.1:c.565+5G=	ENSP00000509447.1:n.565+5G=
ENST00000693308.1:c.497+5G=	ENSP00000509770.1:n.497+5G=
ENST00000693763.1:n.631+5G=
ENST00000245407.8:c.497+5G= MANE Select	ENSP00000245407.3:n.497+5G=
ENST00000245407.7:c.497+5G=	ENSP00000245407.3:n.497+5G=
ENST00000415928.5:c.266+5G=	ENSP00000388838.1:n.266+5G=
ENST00000435065.6:c.569+5G=	ENSP00000402760.2:n.569+5G=
ENST00000437841.6:c.394-6842G=	ENSP00000400553.1:n.394-6842G=
ENST00000461013.5:n.2259G=
NM_001308122.1:c.569+5G=	NP_001295051.1:n.569+5G=
NM_003060.3:c.497+5G=	NP_003051.1:n.497+5G=
XR_427718.1:n.838+5G=
XR_948290.1:n.838+5G=
XR_948291.1:n.838+5G=
XM_011543590.2:c.-135+5G=	XP_011541892.1:n.-135+5G=
XM_017009778.2:c.-31-5661G=	XP_016865267.1:n.-31-5661G=
XR_001742215.1:n.838+5G=
XR_001742216.1:n.838+5G=
XR_427718.2:n.838+5G=
XR_948290.2:n.838+5G=
XR_948291.2:n.838+5G=
NM_003060.4:c.497+5G= MANE Select	NP_003051.1:n.497+5G=
NM_001308122.2:c.569+5G=	NP_001295051.1:n.569+5G=