Canonical Allele Identifier: CA360807797

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726563A>G (hg19) ; chr5:g.132390871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390871A>G , CM000667.2:g.132390871A>G	GRCh38
NC_000005.9:g.131726563A>G , CM000667.1:g.131726563A>G	GRCh37
NC_000005.8:g.131754462A>G	NCBI36
NG_008982.1:g.26163A>G
NG_008982.2:g.26168A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1075A>G	ENSP00000388838.2:p.Ser359Gly
ENST00000435065.7:c.1306A>G	ENSP00000402760.2:p.Ser436Gly
ENST00000448810.6:c.*86A>G	ENSP00000401860.2:n.*86A>G
ENST00000685543.1:n.1375A>G
ENST00000686757.1:c.*398A>G	ENSP00000510721.1:n.*398A>G
ENST00000687740.1:n.3919A>G
ENST00000688151.1:n.2544A>G
ENST00000689271.1:c.1081A>G	ENSP00000510797.1:p.Ser361Gly
ENST00000690900.1:c.*398A>G	ENSP00000510703.1:n.*398A>G
ENST00000692212.1:n.2846A>G
ENST00000692355.1:c.487A>G
ENST00000692413.1:c.1216A>G	ENSP00000509374.1:p.Ser406Gly
ENST00000692825.1:c.1302A>G	ENSP00000509447.1:n.1302A>G
ENST00000693308.1:c.1282A>G	ENSP00000509770.1:p.Ser428Gly
ENST00000693763.1:n.2394A>G
ENST00000245407.8:c.1234A>G MANE Select	ENSP00000245407.3:p.Ser412Gly
ENST00000245407.7:c.1234A>G	ENSP00000245407.3:p.Ser412Gly
ENST00000435065.6:c.1306A>G	ENSP00000402760.2:p.Ser436Gly
ENST00000447841.5:c.112-1562A>G
ENST00000448810.5:c.496A>G
ENST00000461013.5:n.8656A>G
ENST00000475308.1:n.1912A>G
ENST00000479605.5:n.337A>G
NM_001308122.1:c.1306A>G	NP_001295051.1:p.Ser436Gly
NM_003060.3:c.1234A>G	NP_003051.1:p.Ser412Gly
XM_011543590.1:c.616A>G	XP_011541892.1:p.Ser206Gly
XR_427718.1:n.1594A>G
XR_948290.1:n.1394-1562A>G
XR_948291.1:n.1588A>G
XM_011543590.2:c.616A>G	XP_011541892.1:p.Ser206Gly
XM_017009778.2:c.706A>G	XP_016865267.1:p.Ser236Gly
XR_001742215.1:n.1489A>G
XR_001742216.1:n.1508A>G
XR_427718.2:n.1594A>G
XR_948290.2:n.1394-1562A>G
XR_948291.2:n.1588A>G
NM_003060.4:c.1234A>G MANE Select	NP_003051.1:p.Ser412Gly
NM_001308122.2:c.1306A>G	NP_001295051.1:p.Ser436Gly