Canonical Allele Identifier: CA360807728

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726528G>C (hg19) ; chr5:g.132390836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390836G>C , CM000667.2:g.132390836G>C	GRCh38
NC_000005.9:g.131726528G>C , CM000667.1:g.131726528G>C	GRCh37
NC_000005.8:g.131754427G>C	NCBI36
NG_008982.1:g.26128G>C
NG_008982.2:g.26133G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1040G>C	ENSP00000388838.2:p.Arg347Pro
ENST00000435065.7:c.1271G>C	ENSP00000402760.2:p.Arg424Pro
ENST00000448810.6:c.*51G>C	ENSP00000401860.2:n.*51G>C
ENST00000685543.1:n.1340G>C
ENST00000686757.1:c.*363G>C	ENSP00000510721.1:n.*363G>C
ENST00000687740.1:n.3884G>C
ENST00000688151.1:n.2509G>C
ENST00000689271.1:c.1046G>C	ENSP00000510797.1:p.Arg349Pro
ENST00000690900.1:c.*363G>C	ENSP00000510703.1:n.*363G>C
ENST00000692212.1:n.2811G>C
ENST00000692355.1:c.452G>C
ENST00000692413.1:c.1181G>C	ENSP00000509374.1:p.Arg394Pro
ENST00000692825.1:c.1267G>C	ENSP00000509447.1:n.1267G>C
ENST00000693308.1:c.1247G>C	ENSP00000509770.1:p.Arg416Pro
ENST00000693763.1:n.2359G>C
ENST00000245407.8:c.1199G>C MANE Select	ENSP00000245407.3:p.Arg400Pro
ENST00000245407.7:c.1199G>C	ENSP00000245407.3:p.Arg400Pro
ENST00000435065.6:c.1271G>C	ENSP00000402760.2:p.Arg424Pro
ENST00000447841.5:c.112-1597G>C
ENST00000448810.5:c.461G>C
ENST00000461013.5:n.8621G>C
ENST00000475308.1:n.1877G>C
ENST00000479605.5:n.302G>C
NM_001308122.1:c.1271G>C	NP_001295051.1:p.Arg424Pro
NM_003060.3:c.1199G>C	NP_003051.1:p.Arg400Pro
XM_011543590.1:c.581G>C	XP_011541892.1:p.Arg194Pro
XR_427718.1:n.1559G>C
XR_948290.1:n.1394-1597G>C
XR_948291.1:n.1553G>C
XM_011543590.2:c.581G>C	XP_011541892.1:p.Arg194Pro
XM_017009778.2:c.671G>C	XP_016865267.1:p.Arg224Pro
XR_001742215.1:n.1454G>C
XR_001742216.1:n.1473G>C
XR_427718.2:n.1559G>C
XR_948290.2:n.1394-1597G>C
XR_948291.2:n.1553G>C
NM_003060.4:c.1199G>C MANE Select	NP_003051.1:p.Arg400Pro
NM_001308122.2:c.1271G>C	NP_001295051.1:p.Arg424Pro