Canonical Allele Identifier: CA1583151552

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392322T= , CM000667.2:g.132392322T=	GRCh38
NC_000005.9:g.131728014T= , CM000667.1:g.131728014T=	GRCh37
NC_000005.8:g.131755913T=	NCBI36
NG_008982.1:g.27614T=
NG_008982.2:g.27619T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1109-111T=	ENSP00000388838.2:n.1109-111T=
ENST00000435065.7:c.1340-111T=	ENSP00000402760.2:n.1340-111T=
ENST00000448810.6:c.*120-111T=	ENSP00000401860.2:n.*120-111T=
ENST00000685543.1:n.1409-111T=
ENST00000686757.1:c.*432-111T=	ENSP00000510721.1:n.*432-111T=
ENST00000687740.1:n.3953-111T=
ENST00000688151.1:n.2578-111T=
ENST00000689271.1:c.1115-111T=	ENSP00000510797.1:n.1115-111T=
ENST00000690900.1:c.*432-111T=	ENSP00000510703.1:n.*432-111T=
ENST00000692212.1:n.4297T=
ENST00000692355.1:c.521-111T=
ENST00000692413.1:c.1250-111T=	ENSP00000509374.1:n.1250-111T=
ENST00000692825.1:c.1336-111T=	ENSP00000509447.1:n.1336-111T=
ENST00000693308.1:c.1316-111T=	ENSP00000509770.1:n.1316-111T=
ENST00000693763.1:n.2428-111T=
ENST00000245407.8:c.1268-111T= MANE Select	ENSP00000245407.3:n.1268-111T=
ENST00000245407.7:c.1268-111T=	ENSP00000245407.3:n.1268-111T=
ENST00000435065.6:c.1340-111T=	ENSP00000402760.2:n.1340-111T=
ENST00000447841.5:c.112-111T=
ENST00000448810.5:c.530-111T=
ENST00000461013.5:n.8690-111T=
ENST00000475308.1:n.1946-111T=
ENST00000479605.5:n.371-111T=
NM_001308122.1:c.1340-111T=	NP_001295051.1:n.1340-111T=
NM_003060.3:c.1268-111T=	NP_003051.1:n.1268-111T=
XM_011543590.1:c.650-111T=	XP_011541892.1:n.650-111T=
XR_427718.1:n.1628-111T=
XR_948290.1:n.1394-111T=
XR_948291.1:n.1622-111T=
XM_011543590.2:c.650-111T=	XP_011541892.1:n.650-111T=
XM_017009778.2:c.740-111T=	XP_016865267.1:n.740-111T=
XR_001742215.1:n.1523-111T=
XR_001742216.1:n.1542-111T=
XR_427718.2:n.1628-111T=
XR_948290.2:n.1394-111T=
XR_948291.2:n.1622-111T=
NM_003060.4:c.1268-111T= MANE Select	NP_003051.1:n.1268-111T=
NM_001308122.2:c.1340-111T=	NP_001295051.1:n.1340-111T=