Canonical Allele Identifier: CA2675202273

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132389028-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132389028A>G , CM000667.2:g.132389028A>G	GRCh38
NC_000005.9:g.131724720A>G , CM000667.1:g.131724720A>G	GRCh37
NC_000005.8:g.131752619A>G	NCBI36
NG_008982.1:g.24320A>G
NG_008982.2:g.24325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.893+7A>G	ENSP00000388838.2:n.893+7A>G
ENST00000435065.7:c.1124+7A>G	ENSP00000402760.2:n.1124+7A>G
ENST00000448810.6:c.1052+7A>G	ENSP00000401860.2:n.1052+7A>G
ENST00000685543.1:n.1193+7A>G
ENST00000686757.1:c.*216+7A>G	ENSP00000510721.1:n.*216+7A>G
ENST00000687740.1:n.3737+7A>G
ENST00000688151.1:n.2362+7A>G
ENST00000689271.1:c.899+7A>G	ENSP00000510797.1:n.899+7A>G
ENST00000690900.1:c.*216+7A>G	ENSP00000510703.1:n.*216+7A>G
ENST00000692212.1:n.1003A>G
ENST00000692355.1:c.305+7A>G
ENST00000692413.1:c.1034+7A>G	ENSP00000509374.1:n.1034+7A>G
ENST00000692825.1:c.1120+7A>G	ENSP00000509447.1:n.1120+7A>G
ENST00000693308.1:c.1100+7A>G	ENSP00000509770.1:n.1100+7A>G
ENST00000693763.1:n.2212+7A>G
ENST00000245407.8:c.1052+7A>G MANE Select	ENSP00000245407.3:n.1052+7A>G
ENST00000245407.7:c.1052+7A>G	ENSP00000245407.3:n.1052+7A>G
ENST00000435065.6:c.1124+7A>G	ENSP00000402760.2:n.1124+7A>G
ENST00000447841.5:c.111+7A>G
ENST00000448810.5:c.400+7A>G
ENST00000461013.5:n.8474+7A>G
ENST00000475308.1:n.69A>G
ENST00000479605.5:n.155+7A>G
NM_001308122.1:c.1124+7A>G	NP_001295051.1:n.1124+7A>G
NM_003060.3:c.1052+7A>G	NP_003051.1:n.1052+7A>G
XM_011543590.1:c.434+7A>G	XP_011541892.1:n.434+7A>G
XR_427718.1:n.1412+7A>G
XR_948290.1:n.1393+7A>G
XR_948291.1:n.1406+7A>G
XM_011543590.2:c.434+7A>G	XP_011541892.1:n.434+7A>G
XM_017009778.2:c.524+7A>G	XP_016865267.1:n.524+7A>G
XR_001742215.1:n.1393+7A>G
XR_001742216.1:n.1412+7A>G
XR_427718.2:n.1412+7A>G
XR_948290.2:n.1393+7A>G
XR_948291.2:n.1406+7A>G
NM_003060.4:c.1052+7A>G MANE Select	NP_003051.1:n.1052+7A>G
NM_001308122.2:c.1124+7A>G	NP_001295051.1:n.1124+7A>G