Canonical Allele Identifier: CA1583144387

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132384997T= , CM000667.2:g.132384997T=	GRCh38
NC_000005.9:g.131720689T= , CM000667.1:g.131720689T=	GRCh37
NC_000005.8:g.131748588T=	NCBI36
NG_008982.1:g.20289T=
NG_008982.2:g.20294T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+683T=	ENSP00000388838.2:n.665+683T=
ENST00000435065.7:c.725-331T=	ENSP00000402760.2:n.725-331T=
ENST00000448810.6:c.653-331T=	ENSP00000401860.2:n.653-331T=
ENST00000686757.1:c.672-331T=	ENSP00000510721.1:n.672-331T=
ENST00000687740.1:n.1482T=
ENST00000688151.1:n.1845-331T=
ENST00000689271.1:c.671+677T=	ENSP00000510797.1:n.671+677T=
ENST00000690900.1:c.672-379T=	ENSP00000510703.1:n.672-379T=
ENST00000692212.1:n.148T=
ENST00000692355.1:c.204+696T=
ENST00000692413.1:c.672-331T=	ENSP00000509374.1:n.672-331T=
ENST00000692825.1:c.721-331T=	ENSP00000509447.1:n.721-331T=
ENST00000693308.1:c.666-331T=	ENSP00000509770.1:n.666-331T=
ENST00000693763.1:n.1482T=
ENST00000245407.8:c.653-331T= MANE Select	ENSP00000245407.3:n.653-331T=
ENST00000245407.7:c.653-331T=	ENSP00000245407.3:n.653-331T=
ENST00000415928.5:c.422-331T=	ENSP00000388838.1:n.422-331T=
ENST00000435065.6:c.725-331T=	ENSP00000402760.2:n.725-331T=
ENST00000437841.6:c.394-331T=	ENSP00000400553.1:n.394-331T=
ENST00000461013.5:n.8075-331T=
NM_001308122.1:c.725-331T=	NP_001295051.1:n.725-331T=
NM_003060.3:c.653-331T=	NP_003051.1:n.653-331T=
XM_011543590.1:c.35-331T=	XP_011541892.1:n.35-331T=
XR_427718.1:n.1013-331T=
XR_948290.1:n.994-331T=
XR_948291.1:n.1007-331T=
XM_011543590.2:c.35-331T=	XP_011541892.1:n.35-331T=
XM_017009778.2:c.125-331T=	XP_016865267.1:n.125-331T=
XR_001742215.1:n.994-331T=
XR_001742216.1:n.1013-331T=
XR_427718.2:n.1013-331T=
XR_948290.2:n.994-331T=
XR_948291.2:n.1007-331T=
NM_003060.4:c.653-331T= MANE Select	NP_003051.1:n.653-331T=
NM_001308122.2:c.725-331T=	NP_001295051.1:n.725-331T=