Canonical Allele Identifier: CA360807784

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726555T>C (hg19) ; chr5:g.132390863T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390863T>C , CM000667.2:g.132390863T>C	GRCh38
NC_000005.9:g.131726555T>C , CM000667.1:g.131726555T>C	GRCh37
NC_000005.8:g.131754454T>C	NCBI36
NG_008982.1:g.26155T>C
NG_008982.2:g.26160T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1067T>C	ENSP00000388838.2:p.Leu356Pro
ENST00000435065.7:c.1298T>C	ENSP00000402760.2:p.Leu433Pro
ENST00000448810.6:c.*78T>C	ENSP00000401860.2:n.*78T>C
ENST00000685543.1:n.1367T>C
ENST00000686757.1:c.*390T>C	ENSP00000510721.1:n.*390T>C
ENST00000687740.1:n.3911T>C
ENST00000688151.1:n.2536T>C
ENST00000689271.1:c.1073T>C	ENSP00000510797.1:p.Leu358Pro
ENST00000690900.1:c.*390T>C	ENSP00000510703.1:n.*390T>C
ENST00000692212.1:n.2838T>C
ENST00000692355.1:c.479T>C
ENST00000692413.1:c.1208T>C	ENSP00000509374.1:p.Leu403Pro
ENST00000692825.1:c.1294T>C	ENSP00000509447.1:n.1294T>C
ENST00000693308.1:c.1274T>C	ENSP00000509770.1:p.Leu425Pro
ENST00000693763.1:n.2386T>C
ENST00000245407.8:c.1226T>C MANE Select	ENSP00000245407.3:p.Leu409Pro
ENST00000245407.7:c.1226T>C	ENSP00000245407.3:p.Leu409Pro
ENST00000435065.6:c.1298T>C	ENSP00000402760.2:p.Leu433Pro
ENST00000447841.5:c.112-1570T>C
ENST00000448810.5:c.488T>C
ENST00000461013.5:n.8648T>C
ENST00000475308.1:n.1904T>C
ENST00000479605.5:n.329T>C
NM_001308122.1:c.1298T>C	NP_001295051.1:p.Leu433Pro
NM_003060.3:c.1226T>C	NP_003051.1:p.Leu409Pro
XM_011543590.1:c.608T>C	XP_011541892.1:p.Leu203Pro
XR_427718.1:n.1586T>C
XR_948290.1:n.1394-1570T>C
XR_948291.1:n.1580T>C
XM_011543590.2:c.608T>C	XP_011541892.1:p.Leu203Pro
XM_017009778.2:c.698T>C	XP_016865267.1:p.Leu233Pro
XR_001742215.1:n.1481T>C
XR_001742216.1:n.1500T>C
XR_427718.2:n.1586T>C
XR_948290.2:n.1394-1570T>C
XR_948291.2:n.1580T>C
NM_003060.4:c.1226T>C MANE Select	NP_003051.1:p.Leu409Pro
NM_001308122.2:c.1298T>C	NP_001295051.1:p.Leu433Pro