Canonical Allele Identifier: CA446337413

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726397G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390705G>A , CM000667.2:g.132390705G>A	GRCh38
NC_000005.9:g.131726397G>A , CM000667.1:g.131726397G>A	GRCh37
NC_000005.8:g.131754296G>A	NCBI36
NG_008982.1:g.25997G>A
NG_008982.2:g.26002G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.909G>A	ENSP00000388838.2:p.Val303=
ENST00000435065.7:c.1140G>A	ENSP00000402760.2:p.Val380=
ENST00000448810.6:c.1053-71G>A	ENSP00000401860.2:n.1053-71G>A
ENST00000685543.1:n.1209G>A
ENST00000686757.1:c.*232G>A	ENSP00000510721.1:n.*232G>A
ENST00000687740.1:n.3753G>A
ENST00000688151.1:n.2378G>A
ENST00000689271.1:c.915G>A	ENSP00000510797.1:p.Val305=
ENST00000690900.1:c.*232G>A	ENSP00000510703.1:n.*232G>A
ENST00000692212.1:n.2680G>A
ENST00000692355.1:c.321G>A
ENST00000692413.1:c.1050G>A	ENSP00000509374.1:p.Val350=
ENST00000692825.1:c.1136G>A	ENSP00000509447.1:n.1136G>A
ENST00000693308.1:c.1116G>A	ENSP00000509770.1:p.Val372=
ENST00000693763.1:n.2228G>A
ENST00000245407.8:c.1068G>A MANE Select	ENSP00000245407.3:p.Val356=
ENST00000245407.7:c.1068G>A	ENSP00000245407.3:p.Val356=
ENST00000435065.6:c.1140G>A	ENSP00000402760.2:p.Val380=
ENST00000447841.5:c.111+1684G>A
ENST00000448810.5:c.401-71G>A
ENST00000461013.5:n.8490G>A
ENST00000475308.1:n.1746G>A
ENST00000479605.5:n.171G>A
NM_001308122.1:c.1140G>A	NP_001295051.1:p.Val380=
NM_003060.3:c.1068G>A	NP_003051.1:p.Val356=
XM_011543590.1:c.450G>A	XP_011541892.1:p.Val150=
XR_427718.1:n.1428G>A
XR_948290.1:n.1393+1684G>A
XR_948291.1:n.1422G>A
XM_011543590.2:c.450G>A	XP_011541892.1:p.Val150=
XM_017009778.2:c.540G>A	XP_016865267.1:p.Val180=
XR_001742215.1:n.1394-71G>A
XR_001742216.1:n.1413-71G>A
XR_427718.2:n.1428G>A
XR_948290.2:n.1393+1684G>A
XR_948291.2:n.1422G>A
NM_003060.4:c.1068G>A MANE Select	NP_003051.1:p.Val356=
NM_001308122.2:c.1140G>A	NP_001295051.1:p.Val380=