Canonical Allele Identifier: CA1583144512

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393735A= , CM000667.2:g.132393735A=	GRCh38
NC_000005.9:g.131729427A= , CM000667.1:g.131729427A=	GRCh37
NC_000005.8:g.131757326A=	NCBI36
NG_008982.1:g.29027A=
NG_008982.2:g.29032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-450A=	ENSP00000388838.2:n.1292-450A=
ENST00000435065.7:c.1582A=	ENSP00000402760.2:p.Ile528=
ENST00000448810.6:c.*362A=	ENSP00000401860.2:n.*362A=
ENST00000685543.1:n.1651A=
ENST00000686757.1:c.*674A=	ENSP00000510721.1:n.*674A=
ENST00000686868.1:n.502A=
ENST00000687740.1:n.4195A=
ENST00000688151.1:n.2820A=
ENST00000689271.1:c.1357A=	ENSP00000510797.1:p.Ile453=
ENST00000690900.1:c.*674A=	ENSP00000510703.1:n.*674A=
ENST00000692212.1:n.4650A=
ENST00000692355.1:c.763A=
ENST00000692413.1:c.1492A=	ENSP00000509374.1:p.Ile498=
ENST00000692825.1:c.1578A=	ENSP00000509447.1:n.1578A=
ENST00000693308.1:c.1558A=	ENSP00000509770.1:p.Ile520=
ENST00000693763.1:n.2670A=
ENST00000245407.8:c.1510A= MANE Select	ENSP00000245407.3:p.Ile504=
ENST00000245407.7:c.1510A=	ENSP00000245407.3:p.Ile504=
ENST00000435065.6:c.1582A=	ENSP00000402760.2:p.Ile528=
ENST00000447841.5:c.354A=
ENST00000448810.5:c.772A=
ENST00000461013.5:n.8932A=
ENST00000475308.1:n.2188A=
NM_001308122.1:c.1582A=	NP_001295051.1:p.Ile528=
NM_003060.3:c.1510A=	NP_003051.1:p.Ile504=
XM_011543590.1:c.892A=	XP_011541892.1:p.Ile298=
XR_948290.1:n.1636A=
XM_011543590.2:c.892A=	XP_011541892.1:p.Ile298=
XM_017009778.2:c.982A=	XP_016865267.1:p.Ile328=
XR_001742215.1:n.1765A=
XR_001742216.1:n.1784A=
XR_427718.2:n.1870A=
XR_948290.2:n.1636A=
XR_948291.2:n.1864A=
NM_003060.4:c.1510A= MANE Select	NP_003051.1:p.Ile504=
NM_001308122.2:c.1582A=	NP_001295051.1:p.Ile528=