Canonical Allele Identifier: CA446332604

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131722735C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132387043C>A , CM000667.2:g.132387043C>A	GRCh38
NC_000005.9:g.131722735C>A , CM000667.1:g.131722735C>A	GRCh37
NC_000005.8:g.131750634C>A	NCBI36
NG_008982.1:g.22335C>A
NG_008982.2:g.22340C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.684C>A	ENSP00000388838.2:p.Pro228=
ENST00000435065.7:c.915C>A	ENSP00000402760.2:p.Pro305=
ENST00000448810.6:c.843C>A	ENSP00000401860.2:p.Pro281=
ENST00000686757.1:c.*7C>A	ENSP00000510721.1:n.*7C>A
ENST00000687740.1:n.3528C>A
ENST00000688151.1:n.2153C>A
ENST00000689271.1:c.690C>A	ENSP00000510797.1:p.Pro230=
ENST00000690900.1:c.*7C>A	ENSP00000510703.1:n.*7C>A
ENST00000692212.1:n.787C>A
ENST00000692355.1:c.205-1878C>A
ENST00000692413.1:c.844-19C>A	ENSP00000509374.1:n.844-19C>A
ENST00000692825.1:c.911C>A	ENSP00000509447.1:n.911C>A
ENST00000693308.1:c.891C>A	ENSP00000509770.1:p.Pro297=
ENST00000693763.1:n.2003C>A
ENST00000245407.8:c.843C>A MANE Select	ENSP00000245407.3:p.Pro281=
ENST00000245407.7:c.843C>A	ENSP00000245407.3:p.Pro281=
ENST00000415928.5:c.612C>A	ENSP00000388838.1:p.Pro204=
ENST00000435065.6:c.915C>A	ENSP00000402760.2:p.Pro305=
ENST00000437841.6:c.*158C>A	ENSP00000400553.1:n.*158C>A
ENST00000448810.5:c.191C>A
ENST00000461013.5:n.8265C>A
NM_001308122.1:c.915C>A	NP_001295051.1:p.Pro305=
NM_003060.3:c.843C>A	NP_003051.1:p.Pro281=
XM_011543590.1:c.225C>A	XP_011541892.1:p.Pro75=
XR_427718.1:n.1203C>A
XR_948290.1:n.1184C>A
XR_948291.1:n.1197C>A
XM_011543590.2:c.225C>A	XP_011541892.1:p.Pro75=
XM_017009778.2:c.315C>A	XP_016865267.1:p.Pro105=
XR_001742215.1:n.1184C>A
XR_001742216.1:n.1203C>A
XR_427718.2:n.1203C>A
XR_948290.2:n.1184C>A
XR_948291.2:n.1197C>A
NM_003060.4:c.843C>A MANE Select	NP_003051.1:p.Pro281=
NM_001308122.2:c.915C>A	NP_001295051.1:p.Pro305=