Canonical Allele Identifier: CA360807715

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726520G>C (hg19) ; chr5:g.132390828G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390828G>C , CM000667.2:g.132390828G>C	GRCh38
NC_000005.9:g.131726520G>C , CM000667.1:g.131726520G>C	GRCh37
NC_000005.8:g.131754419G>C	NCBI36
NG_008982.1:g.26120G>C
NG_008982.2:g.26125G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1032G>C	ENSP00000388838.2:p.Leu344Phe
ENST00000435065.7:c.1263G>C	ENSP00000402760.2:p.Leu421Phe
ENST00000448810.6:c.*43G>C	ENSP00000401860.2:n.*43G>C
ENST00000685543.1:n.1332G>C
ENST00000686757.1:c.*355G>C	ENSP00000510721.1:n.*355G>C
ENST00000687740.1:n.3876G>C
ENST00000688151.1:n.2501G>C
ENST00000689271.1:c.1038G>C	ENSP00000510797.1:p.Leu346Phe
ENST00000690900.1:c.*355G>C	ENSP00000510703.1:n.*355G>C
ENST00000692212.1:n.2803G>C
ENST00000692355.1:c.444G>C
ENST00000692413.1:c.1173G>C	ENSP00000509374.1:p.Leu391Phe
ENST00000692825.1:c.1259G>C	ENSP00000509447.1:n.1259G>C
ENST00000693308.1:c.1239G>C	ENSP00000509770.1:p.Leu413Phe
ENST00000693763.1:n.2351G>C
ENST00000245407.8:c.1191G>C MANE Select	ENSP00000245407.3:p.Leu397Phe
ENST00000245407.7:c.1191G>C	ENSP00000245407.3:p.Leu397Phe
ENST00000435065.6:c.1263G>C	ENSP00000402760.2:p.Leu421Phe
ENST00000447841.5:c.112-1605G>C
ENST00000448810.5:c.453G>C
ENST00000461013.5:n.8613G>C
ENST00000475308.1:n.1869G>C
ENST00000479605.5:n.294G>C
NM_001308122.1:c.1263G>C	NP_001295051.1:p.Leu421Phe
NM_003060.3:c.1191G>C	NP_003051.1:p.Leu397Phe
XM_011543590.1:c.573G>C	XP_011541892.1:p.Leu191Phe
XR_427718.1:n.1551G>C
XR_948290.1:n.1394-1605G>C
XR_948291.1:n.1545G>C
XM_011543590.2:c.573G>C	XP_011541892.1:p.Leu191Phe
XM_017009778.2:c.663G>C	XP_016865267.1:p.Leu221Phe
XR_001742215.1:n.1446G>C
XR_001742216.1:n.1465G>C
XR_427718.2:n.1551G>C
XR_948290.2:n.1394-1605G>C
XR_948291.2:n.1545G>C
NM_003060.4:c.1191G>C MANE Select	NP_003051.1:p.Leu397Phe
NM_001308122.2:c.1263G>C	NP_001295051.1:p.Leu421Phe