Canonical Allele Identifier: CA360807433

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726401T>G (hg19) ; chr5:g.132390709T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390709T>G , CM000667.2:g.132390709T>G	GRCh38
NC_000005.9:g.131726401T>G , CM000667.1:g.131726401T>G	GRCh37
NC_000005.8:g.131754300T>G	NCBI36
NG_008982.1:g.26001T>G
NG_008982.2:g.26006T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.913T>G	ENSP00000388838.2:p.Tyr305Asp
ENST00000435065.7:c.1144T>G	ENSP00000402760.2:p.Tyr382Asp
ENST00000448810.6:c.1053-67T>G	ENSP00000401860.2:n.1053-67T>G
ENST00000685543.1:n.1213T>G
ENST00000686757.1:c.*236T>G	ENSP00000510721.1:n.*236T>G
ENST00000687740.1:n.3757T>G
ENST00000688151.1:n.2382T>G
ENST00000689271.1:c.919T>G	ENSP00000510797.1:p.Tyr307Asp
ENST00000690900.1:c.*236T>G	ENSP00000510703.1:n.*236T>G
ENST00000692212.1:n.2684T>G
ENST00000692355.1:c.325T>G
ENST00000692413.1:c.1054T>G	ENSP00000509374.1:p.Tyr352Asp
ENST00000692825.1:c.1140T>G	ENSP00000509447.1:n.1140T>G
ENST00000693308.1:c.1120T>G	ENSP00000509770.1:p.Tyr374Asp
ENST00000693763.1:n.2232T>G
ENST00000245407.8:c.1072T>G MANE Select	ENSP00000245407.3:p.Tyr358Asp
ENST00000245407.7:c.1072T>G	ENSP00000245407.3:p.Tyr358Asp
ENST00000435065.6:c.1144T>G	ENSP00000402760.2:p.Tyr382Asp
ENST00000447841.5:c.111+1688T>G
ENST00000448810.5:c.401-67T>G
ENST00000461013.5:n.8494T>G
ENST00000475308.1:n.1750T>G
ENST00000479605.5:n.175T>G
NM_001308122.1:c.1144T>G	NP_001295051.1:p.Tyr382Asp
NM_003060.3:c.1072T>G	NP_003051.1:p.Tyr358Asp
XM_011543590.1:c.454T>G	XP_011541892.1:p.Tyr152Asp
XR_427718.1:n.1432T>G
XR_948290.1:n.1393+1688T>G
XR_948291.1:n.1426T>G
XM_011543590.2:c.454T>G	XP_011541892.1:p.Tyr152Asp
XM_017009778.2:c.544T>G	XP_016865267.1:p.Tyr182Asp
XR_001742215.1:n.1394-67T>G
XR_001742216.1:n.1413-67T>G
XR_427718.2:n.1432T>G
XR_948290.2:n.1393+1688T>G
XR_948291.2:n.1426T>G
NM_003060.4:c.1072T>G MANE Select	NP_003051.1:p.Tyr358Asp
NM_001308122.2:c.1144T>G	NP_001295051.1:p.Tyr382Asp