Canonical Allele Identifier: CA360807492

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726414C>A (hg19) ; chr5:g.132390722C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390722C>A , CM000667.2:g.132390722C>A	GRCh38
NC_000005.9:g.131726414C>A , CM000667.1:g.131726414C>A	GRCh37
NC_000005.8:g.131754313C>A	NCBI36
NG_008982.1:g.26014C>A
NG_008982.2:g.26019C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.926C>A	ENSP00000388838.2:p.Ser309Ter
ENST00000435065.7:c.1157C>A	ENSP00000402760.2:p.Ser386Ter
ENST00000448810.6:c.1053-54C>A	ENSP00000401860.2:n.1053-54C>A
ENST00000685543.1:n.1226C>A
ENST00000686757.1:c.*249C>A	ENSP00000510721.1:n.*249C>A
ENST00000687740.1:n.3770C>A
ENST00000688151.1:n.2395C>A
ENST00000689271.1:c.932C>A	ENSP00000510797.1:p.Ser311Ter
ENST00000690900.1:c.*249C>A	ENSP00000510703.1:n.*249C>A
ENST00000692212.1:n.2697C>A
ENST00000692355.1:c.338C>A
ENST00000692413.1:c.1067C>A	ENSP00000509374.1:p.Ser356Ter
ENST00000692825.1:c.1153C>A	ENSP00000509447.1:n.1153C>A
ENST00000693308.1:c.1133C>A	ENSP00000509770.1:p.Ser378Ter
ENST00000693763.1:n.2245C>A
ENST00000245407.8:c.1085C>A MANE Select	ENSP00000245407.3:p.Ser362Ter
ENST00000245407.7:c.1085C>A	ENSP00000245407.3:p.Ser362Ter
ENST00000435065.6:c.1157C>A	ENSP00000402760.2:p.Ser386Ter
ENST00000447841.5:c.111+1701C>A
ENST00000448810.5:c.401-54C>A
ENST00000461013.5:n.8507C>A
ENST00000475308.1:n.1763C>A
ENST00000479605.5:n.188C>A
NM_001308122.1:c.1157C>A	NP_001295051.1:p.Ser386Ter
NM_003060.3:c.1085C>A	NP_003051.1:p.Ser362Ter
XM_011543590.1:c.467C>A	XP_011541892.1:p.Ser156Ter
XR_427718.1:n.1445C>A
XR_948290.1:n.1393+1701C>A
XR_948291.1:n.1439C>A
XM_011543590.2:c.467C>A	XP_011541892.1:p.Ser156Ter
XM_017009778.2:c.557C>A	XP_016865267.1:p.Ser186Ter
XR_001742215.1:n.1394-54C>A
XR_001742216.1:n.1413-54C>A
XR_427718.2:n.1445C>A
XR_948290.2:n.1393+1701C>A
XR_948291.2:n.1439C>A
NM_003060.4:c.1085C>A MANE Select	NP_003051.1:p.Ser362Ter
NM_001308122.2:c.1157C>A	NP_001295051.1:p.Ser386Ter