Canonical Allele Identifier: CA360809886

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729451A>C (hg19) ; chr5:g.132393759A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393759A>C , CM000667.2:g.132393759A>C	GRCh38
NC_000005.9:g.131729451A>C , CM000667.1:g.131729451A>C	GRCh37
NC_000005.8:g.131757350A>C	NCBI36
NG_008982.1:g.29051A>C
NG_008982.2:g.29056A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-426A>C	ENSP00000388838.2:n.1292-426A>C
ENST00000435065.7:c.1606A>C	ENSP00000402760.2:p.Ser536Arg
ENST00000448810.6:c.*386A>C	ENSP00000401860.2:n.*386A>C
ENST00000685543.1:n.1675A>C
ENST00000686757.1:c.*698A>C	ENSP00000510721.1:n.*698A>C
ENST00000686868.1:n.526A>C
ENST00000687740.1:n.4219A>C
ENST00000688151.1:n.2844A>C
ENST00000689271.1:c.1381A>C	ENSP00000510797.1:p.Ser461Arg
ENST00000690900.1:c.*698A>C	ENSP00000510703.1:n.*698A>C
ENST00000692212.1:n.4674A>C
ENST00000692355.1:c.787A>C
ENST00000692413.1:c.1516A>C	ENSP00000509374.1:p.Ser506Arg
ENST00000692825.1:c.1602A>C	ENSP00000509447.1:n.1602A>C
ENST00000693308.1:c.1582A>C	ENSP00000509770.1:p.Ser528Arg
ENST00000693763.1:n.2694A>C
ENST00000245407.8:c.1534A>C MANE Select	ENSP00000245407.3:p.Ser512Arg
ENST00000245407.7:c.1534A>C	ENSP00000245407.3:p.Ser512Arg
ENST00000435065.6:c.1606A>C	ENSP00000402760.2:p.Ser536Arg
ENST00000447841.5:c.378A>C
ENST00000448810.5:c.796A>C
ENST00000461013.5:n.8956A>C
ENST00000475308.1:n.2212A>C
NM_001308122.1:c.1606A>C	NP_001295051.1:p.Ser536Arg
NM_003060.3:c.1534A>C	NP_003051.1:p.Ser512Arg
XM_011543590.1:c.916A>C	XP_011541892.1:p.Ser306Arg
XR_948290.1:n.1660A>C
XM_011543590.2:c.916A>C	XP_011541892.1:p.Ser306Arg
XM_017009778.2:c.1006A>C	XP_016865267.1:p.Ser336Arg
XR_001742215.1:n.1789A>C
XR_001742216.1:n.1808A>C
XR_427718.2:n.1894A>C
XR_948290.2:n.1660A>C
XR_948291.2:n.1888A>C
NM_003060.4:c.1534A>C MANE Select	NP_003051.1:p.Ser512Arg
NM_001308122.2:c.1606A>C	NP_001295051.1:p.Ser536Arg