Canonical Allele Identifier: CA2675199867

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132393960-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393960C>A , CM000667.2:g.132393960C>A	GRCh38
NC_000005.9:g.131729652C>A , CM000667.1:g.131729652C>A	GRCh37
NC_000005.8:g.131757551C>A	NCBI36
NG_008982.1:g.29252C>A
NG_008982.2:g.29257C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-225C>A	ENSP00000388838.2:n.1292-225C>A
ENST00000435065.7:c.1658+149C>A	ENSP00000402760.2:n.1658+149C>A
ENST00000448810.6:c.*438+149C>A	ENSP00000401860.2:n.*438+149C>A
ENST00000685543.1:n.1727+149C>A
ENST00000686757.1:c.*750+149C>A	ENSP00000510721.1:n.*750+149C>A
ENST00000686868.1:n.578+149C>A
ENST00000687740.1:n.4271+149C>A
ENST00000688151.1:n.2896+149C>A
ENST00000689271.1:c.1433+149C>A	ENSP00000510797.1:n.1433+149C>A
ENST00000690900.1:c.*750+149C>A	ENSP00000510703.1:n.*750+149C>A
ENST00000692212.1:n.4726+149C>A
ENST00000692355.1:c.839+149C>A
ENST00000692413.1:c.1568+149C>A	ENSP00000509374.1:n.1568+149C>A
ENST00000692825.1:c.1654+149C>A	ENSP00000509447.1:n.1654+149C>A
ENST00000693308.1:c.1634+149C>A	ENSP00000509770.1:n.1634+149C>A
ENST00000693763.1:n.2746+149C>A
ENST00000245407.8:c.1586+149C>A MANE Select	ENSP00000245407.3:n.1586+149C>A
ENST00000245407.7:c.1586+149C>A	ENSP00000245407.3:n.1586+149C>A
ENST00000435065.6:c.1658+149C>A	ENSP00000402760.2:n.1658+149C>A
ENST00000447841.5:c.430+149C>A
ENST00000461013.5:n.9008+149C>A
ENST00000475308.1:n.2264+149C>A
NM_001308122.1:c.1658+149C>A	NP_001295051.1:n.1658+149C>A
NM_003060.3:c.1586+149C>A	NP_003051.1:n.1586+149C>A
XM_011543590.1:c.968+149C>A	XP_011541892.1:n.968+149C>A
XR_948290.1:n.1712+149C>A
XM_011543590.2:c.968+149C>A	XP_011541892.1:n.968+149C>A
XM_017009778.2:c.1058+149C>A	XP_016865267.1:n.1058+149C>A
XR_001742215.1:n.1841+149C>A
XR_001742216.1:n.1860+149C>A
XR_427718.2:n.1946+149C>A
XR_948290.2:n.1712+149C>A
XR_948291.2:n.1940+149C>A
NM_003060.4:c.1586+149C>A MANE Select	NP_003051.1:n.1586+149C>A
NM_001308122.2:c.1658+149C>A	NP_001295051.1:n.1658+149C>A