Canonical Allele Identifier: CA360809949

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729467T>G (hg19) ; chr5:g.132393775T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393775T>G , CM000667.2:g.132393775T>G	GRCh38
NC_000005.9:g.131729467T>G , CM000667.1:g.131729467T>G	GRCh37
NC_000005.8:g.131757366T>G	NCBI36
NG_008982.1:g.29067T>G
NG_008982.2:g.29072T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-410T>G	ENSP00000388838.2:n.1292-410T>G
ENST00000435065.7:c.1622T>G	ENSP00000402760.2:p.Leu541Arg
ENST00000448810.6:c.*402T>G	ENSP00000401860.2:n.*402T>G
ENST00000685543.1:n.1691T>G
ENST00000686757.1:c.*714T>G	ENSP00000510721.1:n.*714T>G
ENST00000686868.1:n.542T>G
ENST00000687740.1:n.4235T>G
ENST00000688151.1:n.2860T>G
ENST00000689271.1:c.1397T>G	ENSP00000510797.1:p.Leu466Arg
ENST00000690900.1:c.*714T>G	ENSP00000510703.1:n.*714T>G
ENST00000692212.1:n.4690T>G
ENST00000692355.1:c.803T>G
ENST00000692413.1:c.1532T>G	ENSP00000509374.1:p.Leu511Arg
ENST00000692825.1:c.1618T>G	ENSP00000509447.1:n.1618T>G
ENST00000693308.1:c.1598T>G	ENSP00000509770.1:p.Leu533Arg
ENST00000693763.1:n.2710T>G
ENST00000245407.8:c.1550T>G MANE Select	ENSP00000245407.3:p.Leu517Arg
ENST00000245407.7:c.1550T>G	ENSP00000245407.3:p.Leu517Arg
ENST00000435065.6:c.1622T>G	ENSP00000402760.2:p.Leu541Arg
ENST00000447841.5:c.394T>G
ENST00000448810.5:c.812T>G
ENST00000461013.5:n.8972T>G
ENST00000475308.1:n.2228T>G
NM_001308122.1:c.1622T>G	NP_001295051.1:p.Leu541Arg
NM_003060.3:c.1550T>G	NP_003051.1:p.Leu517Arg
XM_011543590.1:c.932T>G	XP_011541892.1:p.Leu311Arg
XR_948290.1:n.1676T>G
XM_011543590.2:c.932T>G	XP_011541892.1:p.Leu311Arg
XM_017009778.2:c.1022T>G	XP_016865267.1:p.Leu341Arg
XR_001742215.1:n.1805T>G
XR_001742216.1:n.1824T>G
XR_427718.2:n.1910T>G
XR_948290.2:n.1676T>G
XR_948291.2:n.1904T>G
NM_003060.4:c.1550T>G MANE Select	NP_003051.1:p.Leu517Arg
NM_001308122.2:c.1622T>G	NP_001295051.1:p.Leu541Arg