Canonical Allele Identifier: CA360809938

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131729464C>A (hg19) ; chr5:g.132393772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393772C>A , CM000667.2:g.132393772C>A	GRCh38
NC_000005.9:g.131729464C>A , CM000667.1:g.131729464C>A	GRCh37
NC_000005.8:g.131757363C>A	NCBI36
NG_008982.1:g.29064C>A
NG_008982.2:g.29069C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-413C>A	ENSP00000388838.2:n.1292-413C>A
ENST00000435065.7:c.1619C>A	ENSP00000402760.2:p.Pro540Gln
ENST00000448810.6:c.*399C>A	ENSP00000401860.2:n.*399C>A
ENST00000685543.1:n.1688C>A
ENST00000686757.1:c.*711C>A	ENSP00000510721.1:n.*711C>A
ENST00000686868.1:n.539C>A
ENST00000687740.1:n.4232C>A
ENST00000688151.1:n.2857C>A
ENST00000689271.1:c.1394C>A	ENSP00000510797.1:p.Pro465Gln
ENST00000690900.1:c.*711C>A	ENSP00000510703.1:n.*711C>A
ENST00000692212.1:n.4687C>A
ENST00000692355.1:c.800C>A
ENST00000692413.1:c.1529C>A	ENSP00000509374.1:p.Pro510Gln
ENST00000692825.1:c.1615C>A	ENSP00000509447.1:n.1615C>A
ENST00000693308.1:c.1595C>A	ENSP00000509770.1:p.Pro532Gln
ENST00000693763.1:n.2707C>A
ENST00000245407.8:c.1547C>A MANE Select	ENSP00000245407.3:p.Pro516Gln
ENST00000245407.7:c.1547C>A	ENSP00000245407.3:p.Pro516Gln
ENST00000435065.6:c.1619C>A	ENSP00000402760.2:p.Pro540Gln
ENST00000447841.5:c.391C>A
ENST00000448810.5:c.809C>A
ENST00000461013.5:n.8969C>A
ENST00000475308.1:n.2225C>A
NM_001308122.1:c.1619C>A	NP_001295051.1:p.Pro540Gln
NM_003060.3:c.1547C>A	NP_003051.1:p.Pro516Gln
XM_011543590.1:c.929C>A	XP_011541892.1:p.Pro310Gln
XR_948290.1:n.1673C>A
XM_011543590.2:c.929C>A	XP_011541892.1:p.Pro310Gln
XM_017009778.2:c.1019C>A	XP_016865267.1:p.Pro340Gln
XR_001742215.1:n.1802C>A
XR_001742216.1:n.1821C>A
XR_427718.2:n.1907C>A
XR_948290.2:n.1673C>A
XR_948291.2:n.1901C>A
NM_003060.4:c.1547C>A MANE Select	NP_003051.1:p.Pro516Gln
NM_001308122.2:c.1619C>A	NP_001295051.1:p.Pro540Gln