Canonical Allele Identifier: CA1583151827

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392498A= , CM000667.2:g.132392498A=	GRCh38
NC_000005.9:g.131728190A= , CM000667.1:g.131728190A=	GRCh37
NC_000005.8:g.131756089A=	NCBI36
NG_008982.1:g.27790A=
NG_008982.2:g.27795A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1174A=	ENSP00000388838.2:p.Met392=
ENST00000435065.7:c.1405A=	ENSP00000402760.2:p.Met469=
ENST00000448810.6:c.*185A=	ENSP00000401860.2:n.*185A=
ENST00000685543.1:n.1474A=
ENST00000686757.1:c.*497A=	ENSP00000510721.1:n.*497A=
ENST00000687740.1:n.4018A=
ENST00000688151.1:n.2643A=
ENST00000689271.1:c.1180A=	ENSP00000510797.1:p.Met394=
ENST00000690900.1:c.*497A=	ENSP00000510703.1:n.*497A=
ENST00000692212.1:n.4473A=
ENST00000692355.1:c.586A=
ENST00000692413.1:c.1315A=	ENSP00000509374.1:p.Met439=
ENST00000692825.1:c.1401A=	ENSP00000509447.1:n.1401A=
ENST00000693308.1:c.1381A=	ENSP00000509770.1:p.Met461=
ENST00000693763.1:n.2493A=
ENST00000245407.8:c.1333A= MANE Select	ENSP00000245407.3:p.Met445=
ENST00000245407.7:c.1333A=	ENSP00000245407.3:p.Met445=
ENST00000435065.6:c.1405A=	ENSP00000402760.2:p.Met469=
ENST00000447841.5:c.177A=
ENST00000448810.5:c.595A=
ENST00000461013.5:n.8755A=
ENST00000475308.1:n.2011A=
ENST00000479605.5:n.436A=
NM_001308122.1:c.1405A=	NP_001295051.1:p.Met469=
NM_003060.3:c.1333A=	NP_003051.1:p.Met445=
XM_011543590.1:c.715A=	XP_011541892.1:p.Met239=
XR_948290.1:n.1459A=
XM_011543590.2:c.715A=	XP_011541892.1:p.Met239=
XM_017009778.2:c.805A=	XP_016865267.1:p.Met269=
XR_001742215.1:n.1588A=
XR_001742216.1:n.1607A=
XR_427718.2:n.1693A=
XR_948290.2:n.1459A=
XR_948291.2:n.1687A=
NM_003060.4:c.1333A= MANE Select	NP_003051.1:p.Met445=
NM_001308122.2:c.1405A=	NP_001295051.1:p.Met469=