Canonical Allele Identifier: CA1583144793

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132394186A= , CM000667.2:g.132394186A=	GRCh38
NC_000005.9:g.131729878A= , CM000667.1:g.131729878A=	GRCh37
NC_000005.8:g.131757777A=	NCBI36
NG_008982.1:g.29478A=
NG_008982.2:g.29483A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1293A=	ENSP00000388838.2:p.Glu431=
ENST00000435065.7:c.1660A=	ENSP00000402760.2:p.Met554=
ENST00000448810.6:c.*440A=	ENSP00000401860.2:n.*440A=
ENST00000685543.1:n.1729A=
ENST00000686757.1:c.*752A=	ENSP00000510721.1:n.*752A=
ENST00000686868.1:n.580A=
ENST00000687740.1:n.4273A=
ENST00000688151.1:n.2898A=
ENST00000689271.1:c.1435A=	ENSP00000510797.1:p.Met479=
ENST00000690900.1:c.*752A=	ENSP00000510703.1:n.*752A=
ENST00000692212.1:n.4728A=
ENST00000692355.1:c.841A=
ENST00000692413.1:c.1570A=	ENSP00000509374.1:p.Met524=
ENST00000692825.1:c.1656A=	ENSP00000509447.1:n.1656A=
ENST00000693308.1:c.1636A=	ENSP00000509770.1:p.Met546=
ENST00000693763.1:n.2748A=
ENST00000245407.8:c.1588A= MANE Select	ENSP00000245407.3:p.Met530=
ENST00000245407.7:c.1588A=	ENSP00000245407.3:p.Met530=
ENST00000435065.6:c.1660A=	ENSP00000402760.2:p.Met554=
ENST00000447841.5:c.432A=
ENST00000461013.5:n.9010A=
ENST00000475308.1:n.2266A=
NM_001308122.1:c.1660A=	NP_001295051.1:p.Met554=
NM_003060.3:c.1588A=	NP_003051.1:p.Met530=
XM_011543590.1:c.970A=	XP_011541892.1:p.Met324=
XR_948290.1:n.1714A=
XM_011543590.2:c.970A=	XP_011541892.1:p.Met324=
XM_017009778.2:c.1060A=	XP_016865267.1:p.Met354=
XR_001742215.1:n.1843A=
XR_001742216.1:n.1862A=
XR_427718.2:n.1948A=
XR_948290.2:n.1714A=
XR_948291.2:n.1942A=
NM_003060.4:c.1588A= MANE Select	NP_003051.1:p.Met530=
NM_001308122.2:c.1660A=	NP_001295051.1:p.Met554=