Canonical Allele Identifier: CA446337481

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1580892200
• MyVariant Identifiers: chr5:g.131726403T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390711T>C , CM000667.2:g.132390711T>C	GRCh38
NC_000005.9:g.131726403T>C , CM000667.1:g.131726403T>C	GRCh37
NC_000005.8:g.131754302T>C	NCBI36
NG_008982.1:g.26003T>C
NG_008982.2:g.26008T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.915T>C	ENSP00000388838.2:p.Tyr305=
ENST00000435065.7:c.1146T>C	ENSP00000402760.2:p.Tyr382=
ENST00000448810.6:c.1053-65T>C	ENSP00000401860.2:n.1053-65T>C
ENST00000685543.1:n.1215T>C
ENST00000686757.1:c.*238T>C	ENSP00000510721.1:n.*238T>C
ENST00000687740.1:n.3759T>C
ENST00000688151.1:n.2384T>C
ENST00000689271.1:c.921T>C	ENSP00000510797.1:p.Tyr307=
ENST00000690900.1:c.*238T>C	ENSP00000510703.1:n.*238T>C
ENST00000692212.1:n.2686T>C
ENST00000692355.1:c.327T>C
ENST00000692413.1:c.1056T>C	ENSP00000509374.1:p.Tyr352=
ENST00000692825.1:c.1142T>C	ENSP00000509447.1:n.1142T>C
ENST00000693308.1:c.1122T>C	ENSP00000509770.1:p.Tyr374=
ENST00000693763.1:n.2234T>C
ENST00000245407.8:c.1074T>C MANE Select	ENSP00000245407.3:p.Tyr358=
ENST00000245407.7:c.1074T>C	ENSP00000245407.3:p.Tyr358=
ENST00000435065.6:c.1146T>C	ENSP00000402760.2:p.Tyr382=
ENST00000447841.5:c.111+1690T>C
ENST00000448810.5:c.401-65T>C
ENST00000461013.5:n.8496T>C
ENST00000475308.1:n.1752T>C
ENST00000479605.5:n.177T>C
NM_001308122.1:c.1146T>C	NP_001295051.1:p.Tyr382=
NM_003060.3:c.1074T>C	NP_003051.1:p.Tyr358=
XM_011543590.1:c.456T>C	XP_011541892.1:p.Tyr152=
XR_427718.1:n.1434T>C
XR_948290.1:n.1393+1690T>C
XR_948291.1:n.1428T>C
XM_011543590.2:c.456T>C	XP_011541892.1:p.Tyr152=
XM_017009778.2:c.546T>C	XP_016865267.1:p.Tyr182=
XR_001742215.1:n.1394-65T>C
XR_001742216.1:n.1413-65T>C
XR_427718.2:n.1434T>C
XR_948290.2:n.1393+1690T>C
XR_948291.2:n.1428T>C
NM_003060.4:c.1074T>C MANE Select	NP_003051.1:p.Tyr358=
NM_001308122.2:c.1146T>C	NP_001295051.1:p.Tyr382=