Canonical Allele Identifier: CA446342900

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131728180T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132392488T>A , CM000667.2:g.132392488T>A	GRCh38
NC_000005.9:g.131728180T>A , CM000667.1:g.131728180T>A	GRCh37
NC_000005.8:g.131756079T>A	NCBI36
NG_008982.1:g.27780T>A
NG_008982.2:g.27785T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1164T>A	ENSP00000388838.2:p.Ala388=
ENST00000435065.7:c.1395T>A	ENSP00000402760.2:p.Ala465=
ENST00000448810.6:c.*175T>A	ENSP00000401860.2:n.*175T>A
ENST00000685543.1:n.1464T>A
ENST00000686757.1:c.*487T>A	ENSP00000510721.1:n.*487T>A
ENST00000687740.1:n.4008T>A
ENST00000688151.1:n.2633T>A
ENST00000689271.1:c.1170T>A	ENSP00000510797.1:p.Ala390=
ENST00000690900.1:c.*487T>A	ENSP00000510703.1:n.*487T>A
ENST00000692212.1:n.4463T>A
ENST00000692355.1:c.576T>A
ENST00000692413.1:c.1305T>A	ENSP00000509374.1:p.Ala435=
ENST00000692825.1:c.1391T>A	ENSP00000509447.1:n.1391T>A
ENST00000693308.1:c.1371T>A	ENSP00000509770.1:p.Ala457=
ENST00000693763.1:n.2483T>A
ENST00000245407.8:c.1323T>A MANE Select	ENSP00000245407.3:p.Ala441=
ENST00000245407.7:c.1323T>A	ENSP00000245407.3:p.Ala441=
ENST00000435065.6:c.1395T>A	ENSP00000402760.2:p.Ala465=
ENST00000447841.5:c.167T>A
ENST00000448810.5:c.585T>A
ENST00000461013.5:n.8745T>A
ENST00000475308.1:n.2001T>A
ENST00000479605.5:n.426T>A
NM_001308122.1:c.1395T>A	NP_001295051.1:p.Ala465=
NM_003060.3:c.1323T>A	NP_003051.1:p.Ala441=
XM_011543590.1:c.705T>A	XP_011541892.1:p.Ala235=
XR_948290.1:n.1449T>A
XM_011543590.2:c.705T>A	XP_011541892.1:p.Ala235=
XM_017009778.2:c.795T>A	XP_016865267.1:p.Ala265=
XR_001742215.1:n.1578T>A
XR_001742216.1:n.1597T>A
XR_427718.2:n.1683T>A
XR_948290.2:n.1449T>A
XR_948291.2:n.1677T>A
NM_003060.4:c.1323T>A MANE Select	NP_003051.1:p.Ala441=
NM_001308122.2:c.1395T>A	NP_001295051.1:p.Ala465=