Canonical Allele Identifier: CA360807608

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726470A>G (hg19) ; chr5:g.132390778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390778A>G , CM000667.2:g.132390778A>G	GRCh38
NC_000005.9:g.131726470A>G , CM000667.1:g.131726470A>G	GRCh37
NC_000005.8:g.131754369A>G	NCBI36
NG_008982.1:g.26070A>G
NG_008982.2:g.26075A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.982A>G	ENSP00000388838.2:p.Met328Val
ENST00000435065.7:c.1213A>G	ENSP00000402760.2:p.Met405Val
ENST00000448810.6:c.1055A>G	ENSP00000401860.2:p.Asp352Gly
ENST00000685543.1:n.1282A>G
ENST00000686757.1:c.*305A>G	ENSP00000510721.1:n.*305A>G
ENST00000687740.1:n.3826A>G
ENST00000688151.1:n.2451A>G
ENST00000689271.1:c.988A>G	ENSP00000510797.1:p.Met330Val
ENST00000690900.1:c.*305A>G	ENSP00000510703.1:n.*305A>G
ENST00000692212.1:n.2753A>G
ENST00000692355.1:c.394A>G
ENST00000692413.1:c.1123A>G	ENSP00000509374.1:p.Met375Val
ENST00000692825.1:c.1209A>G	ENSP00000509447.1:n.1209A>G
ENST00000693308.1:c.1189A>G	ENSP00000509770.1:p.Met397Val
ENST00000693763.1:n.2301A>G
ENST00000245407.8:c.1141A>G MANE Select	ENSP00000245407.3:p.Met381Val
ENST00000245407.7:c.1141A>G	ENSP00000245407.3:p.Met381Val
ENST00000435065.6:c.1213A>G	ENSP00000402760.2:p.Met405Val
ENST00000447841.5:c.112-1655A>G
ENST00000448810.5:c.403A>G
ENST00000461013.5:n.8563A>G
ENST00000475308.1:n.1819A>G
ENST00000479605.5:n.244A>G
NM_001308122.1:c.1213A>G	NP_001295051.1:p.Met405Val
NM_003060.3:c.1141A>G	NP_003051.1:p.Met381Val
XM_011543590.1:c.523A>G	XP_011541892.1:p.Met175Val
XR_427718.1:n.1501A>G
XR_948290.1:n.1394-1655A>G
XR_948291.1:n.1495A>G
XM_011543590.2:c.523A>G	XP_011541892.1:p.Met175Val
XM_017009778.2:c.613A>G	XP_016865267.1:p.Met205Val
XR_001742215.1:n.1396A>G
XR_001742216.1:n.1415A>G
XR_427718.2:n.1501A>G
XR_948290.2:n.1394-1655A>G
XR_948291.2:n.1495A>G
NM_003060.4:c.1141A>G MANE Select	NP_003051.1:p.Met381Val
NM_001308122.2:c.1213A>G	NP_001295051.1:p.Met405Val