Canonical Allele Identifier: CA360807677

Gene: SLC22A5

Linked Data

• ClinVar Variation Id: 460392
• ClinVar RCV Id: RCV000526345
• dbSNP Id: rs1554088165
• MyVariant Identifiers: chr5:g.131726501G>A (hg19) ; chr5:g.132390809G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390809G>A , CM000667.2:g.132390809G>A	GRCh38
NC_000005.9:g.131726501G>A , CM000667.1:g.131726501G>A	GRCh37
NC_000005.8:g.131754400G>A	NCBI36
NG_008982.1:g.26101G>A
NG_008982.2:g.26106G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1013G>A	ENSP00000388838.2:p.Trp338Ter
ENST00000435065.7:c.1244G>A	ENSP00000402760.2:p.Trp415Ter
ENST00000448810.6:c.*24G>A	ENSP00000401860.2:n.*24G>A
ENST00000685543.1:n.1313G>A
ENST00000686757.1:c.*336G>A	ENSP00000510721.1:n.*336G>A
ENST00000687740.1:n.3857G>A
ENST00000688151.1:n.2482G>A
ENST00000689271.1:c.1019G>A	ENSP00000510797.1:p.Trp340Ter
ENST00000690900.1:c.*336G>A	ENSP00000510703.1:n.*336G>A
ENST00000692212.1:n.2784G>A
ENST00000692355.1:c.425G>A
ENST00000692413.1:c.1154G>A	ENSP00000509374.1:p.Trp385Ter
ENST00000692825.1:c.1240G>A	ENSP00000509447.1:n.1240G>A
ENST00000693308.1:c.1220G>A	ENSP00000509770.1:p.Trp407Ter
ENST00000693763.1:n.2332G>A
ENST00000245407.8:c.1172G>A MANE Select	ENSP00000245407.3:p.Trp391Ter
ENST00000245407.7:c.1172G>A	ENSP00000245407.3:p.Trp391Ter
ENST00000435065.6:c.1244G>A	ENSP00000402760.2:p.Trp415Ter
ENST00000447841.5:c.112-1624G>A
ENST00000448810.5:c.434G>A
ENST00000461013.5:n.8594G>A
ENST00000475308.1:n.1850G>A
ENST00000479605.5:n.275G>A
NM_001308122.1:c.1244G>A	NP_001295051.1:p.Trp415Ter
NM_003060.3:c.1172G>A	NP_003051.1:p.Trp391Ter
XM_011543590.1:c.554G>A	XP_011541892.1:p.Trp185Ter
XR_427718.1:n.1532G>A
XR_948290.1:n.1394-1624G>A
XR_948291.1:n.1526G>A
XM_011543590.2:c.554G>A	XP_011541892.1:p.Trp185Ter
XM_017009778.2:c.644G>A	XP_016865267.1:p.Trp215Ter
XR_001742215.1:n.1427G>A
XR_001742216.1:n.1446G>A
XR_427718.2:n.1532G>A
XR_948290.2:n.1394-1624G>A
XR_948291.2:n.1526G>A
NM_003060.4:c.1172G>A MANE Select	NP_003051.1:p.Trp391Ter
NM_001308122.2:c.1244G>A	NP_001295051.1:p.Trp415Ter