Canonical Allele Identifier: CA446340233

Gene: SLC22A5

Linked Data

• MyVariant Identifiers: chr5:g.131726592C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390900C>A , CM000667.2:g.132390900C>A	GRCh38
NC_000005.9:g.131726592C>A , CM000667.1:g.131726592C>A	GRCh37
NC_000005.8:g.131754491C>A	NCBI36
NG_008982.1:g.26192C>A
NG_008982.2:g.26197C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1104C>A	ENSP00000388838.2:p.Pro368=
ENST00000435065.7:c.1335C>A	ENSP00000402760.2:p.Pro445=
ENST00000448810.6:c.*115C>A	ENSP00000401860.2:n.*115C>A
ENST00000685543.1:n.1404C>A
ENST00000686757.1:c.*427C>A	ENSP00000510721.1:n.*427C>A
ENST00000687740.1:n.3948C>A
ENST00000688151.1:n.2573C>A
ENST00000689271.1:c.1110C>A	ENSP00000510797.1:p.Pro370=
ENST00000690900.1:c.*427C>A	ENSP00000510703.1:n.*427C>A
ENST00000692212.1:n.2875C>A
ENST00000692355.1:c.516C>A
ENST00000692413.1:c.1245C>A	ENSP00000509374.1:p.Pro415=
ENST00000692825.1:c.1331C>A	ENSP00000509447.1:n.1331C>A
ENST00000693308.1:c.1311C>A	ENSP00000509770.1:p.Pro437=
ENST00000693763.1:n.2423C>A
ENST00000245407.8:c.1263C>A MANE Select	ENSP00000245407.3:p.Pro421=
ENST00000245407.7:c.1263C>A	ENSP00000245407.3:p.Pro421=
ENST00000435065.6:c.1335C>A	ENSP00000402760.2:p.Pro445=
ENST00000447841.5:c.112-1533C>A
ENST00000448810.5:c.525C>A
ENST00000461013.5:n.8685C>A
ENST00000475308.1:n.1941C>A
ENST00000479605.5:n.366C>A
NM_001308122.1:c.1335C>A	NP_001295051.1:p.Pro445=
NM_003060.3:c.1263C>A	NP_003051.1:p.Pro421=
XM_011543590.1:c.645C>A	XP_011541892.1:p.Pro215=
XR_427718.1:n.1623C>A
XR_948290.1:n.1394-1533C>A
XR_948291.1:n.1617C>A
XM_011543590.2:c.645C>A	XP_011541892.1:p.Pro215=
XM_017009778.2:c.735C>A	XP_016865267.1:p.Pro245=
XR_001742215.1:n.1518C>A
XR_001742216.1:n.1537C>A
XR_427718.2:n.1623C>A
XR_948290.2:n.1394-1533C>A
XR_948291.2:n.1617C>A
NM_003060.4:c.1263C>A MANE Select	NP_003051.1:p.Pro421=
NM_001308122.2:c.1335C>A	NP_001295051.1:p.Pro445=