Canonical Allele Identifier: CA1583144465

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393700A= , CM000667.2:g.132393700A=	GRCh38
NC_000005.9:g.131729392A= , CM000667.1:g.131729392A=	GRCh37
NC_000005.8:g.131757291A=	NCBI36
NG_008982.1:g.28992A=
NG_008982.2:g.28997A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-485A=	ENSP00000388838.2:n.1292-485A=
ENST00000435065.7:c.1547A=	ENSP00000402760.2:p.Tyr516=
ENST00000448810.6:c.*327A=	ENSP00000401860.2:n.*327A=
ENST00000685543.1:n.1616A=
ENST00000686757.1:c.*639A=	ENSP00000510721.1:n.*639A=
ENST00000686868.1:n.467A=
ENST00000687740.1:n.4160A=
ENST00000688151.1:n.2785A=
ENST00000689271.1:c.1322A=	ENSP00000510797.1:p.Tyr441=
ENST00000690900.1:c.*639A=	ENSP00000510703.1:n.*639A=
ENST00000692212.1:n.4615A=
ENST00000692355.1:c.728A=
ENST00000692413.1:c.1457A=	ENSP00000509374.1:p.Tyr486=
ENST00000692825.1:c.1543A=	ENSP00000509447.1:n.1543A=
ENST00000693308.1:c.1523A=	ENSP00000509770.1:p.Tyr508=
ENST00000693763.1:n.2635A=
ENST00000245407.8:c.1475A= MANE Select	ENSP00000245407.3:p.Tyr492=
ENST00000245407.7:c.1475A=	ENSP00000245407.3:p.Tyr492=
ENST00000435065.6:c.1547A=	ENSP00000402760.2:p.Tyr516=
ENST00000447841.5:c.319A=
ENST00000448810.5:c.737A=
ENST00000461013.5:n.8897A=
ENST00000475308.1:n.2153A=
NM_001308122.1:c.1547A=	NP_001295051.1:p.Tyr516=
NM_003060.3:c.1475A=	NP_003051.1:p.Tyr492=
XM_011543590.1:c.857A=	XP_011541892.1:p.Tyr286=
XR_948290.1:n.1601A=
XM_011543590.2:c.857A=	XP_011541892.1:p.Tyr286=
XM_017009778.2:c.947A=	XP_016865267.1:p.Tyr316=
XR_001742215.1:n.1730A=
XR_001742216.1:n.1749A=
XR_427718.2:n.1835A=
XR_948290.2:n.1601A=
XR_948291.2:n.1829A=
NM_003060.4:c.1475A= MANE Select	NP_003051.1:p.Tyr492=
NM_001308122.2:c.1547A=	NP_001295051.1:p.Tyr516=