Canonical Allele Identifier: CA360810168

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729891A>G (hg19) ; chr5:g.132394199A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132394199A>G , CM000667.2:g.132394199A>G	GRCh38
NC_000005.9:g.131729891A>G , CM000667.1:g.131729891A>G	GRCh37
NC_000005.8:g.131757790A>G	NCBI36
NG_008982.1:g.29491A>G
NG_008982.2:g.29496A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.*10A>G	ENSP00000388838.2:n.*10A>G
ENST00000435065.7:c.1673A>G	ENSP00000402760.2:p.Lys558Arg
ENST00000448810.6:c.*453A>G	ENSP00000401860.2:n.*453A>G
ENST00000685543.1:n.1742A>G
ENST00000686757.1:c.*765A>G	ENSP00000510721.1:n.*765A>G
ENST00000686868.1:n.593A>G
ENST00000687740.1:n.4286A>G
ENST00000688151.1:n.2911A>G
ENST00000689271.1:c.1448A>G	ENSP00000510797.1:p.Lys483Arg
ENST00000690900.1:c.*765A>G	ENSP00000510703.1:n.*765A>G
ENST00000692212.1:n.4741A>G
ENST00000692355.1:c.854A>G
ENST00000692413.1:c.1583A>G	ENSP00000509374.1:p.Lys528Arg
ENST00000692825.1:c.1669A>G	ENSP00000509447.1:n.1669A>G
ENST00000693308.1:c.1649A>G	ENSP00000509770.1:p.Lys550Arg
ENST00000693763.1:n.2761A>G
ENST00000245407.8:c.1601A>G MANE Select	ENSP00000245407.3:p.Lys534Arg
ENST00000245407.7:c.1601A>G	ENSP00000245407.3:p.Lys534Arg
ENST00000435065.6:c.1673A>G	ENSP00000402760.2:p.Lys558Arg
ENST00000447841.5:c.445A>G
ENST00000461013.5:n.9023A>G
ENST00000475308.1:n.2279A>G
NM_001308122.1:c.1673A>G	NP_001295051.1:p.Lys558Arg
NM_003060.3:c.1601A>G	NP_003051.1:p.Lys534Arg
XM_011543590.1:c.983A>G	XP_011541892.1:p.Lys328Arg
XR_948290.1:n.1727A>G
XM_011543590.2:c.983A>G	XP_011541892.1:p.Lys328Arg
XM_017009778.2:c.1073A>G	XP_016865267.1:p.Lys358Arg
XR_001742215.1:n.1856A>G
XR_001742216.1:n.1875A>G
XR_427718.2:n.1961A>G
XR_948290.2:n.1727A>G
XR_948291.2:n.1955A>G
NM_003060.4:c.1601A>G MANE Select	NP_003051.1:p.Lys534Arg
NM_001308122.2:c.1673A>G	NP_001295051.1:p.Lys558Arg