Canonical Allele Identifier: CA2675199820

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132393906-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393906C>G , CM000667.2:g.132393906C>G	GRCh38
NC_000005.9:g.131729598C>G , CM000667.1:g.131729598C>G	GRCh37
NC_000005.8:g.131757497C>G	NCBI36
NG_008982.1:g.29198C>G
NG_008982.2:g.29203C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-279C>G	ENSP00000388838.2:n.1292-279C>G
ENST00000435065.7:c.1658+95C>G	ENSP00000402760.2:n.1658+95C>G
ENST00000448810.6:c.*438+95C>G	ENSP00000401860.2:n.*438+95C>G
ENST00000685543.1:n.1727+95C>G
ENST00000686757.1:c.*750+95C>G	ENSP00000510721.1:n.*750+95C>G
ENST00000686868.1:n.578+95C>G
ENST00000687740.1:n.4271+95C>G
ENST00000688151.1:n.2896+95C>G
ENST00000689271.1:c.1433+95C>G	ENSP00000510797.1:n.1433+95C>G
ENST00000690900.1:c.*750+95C>G	ENSP00000510703.1:n.*750+95C>G
ENST00000692212.1:n.4726+95C>G
ENST00000692355.1:c.839+95C>G
ENST00000692413.1:c.1568+95C>G	ENSP00000509374.1:n.1568+95C>G
ENST00000692825.1:c.1654+95C>G	ENSP00000509447.1:n.1654+95C>G
ENST00000693308.1:c.1634+95C>G	ENSP00000509770.1:n.1634+95C>G
ENST00000693763.1:n.2746+95C>G
ENST00000245407.8:c.1586+95C>G MANE Select	ENSP00000245407.3:n.1586+95C>G
ENST00000245407.7:c.1586+95C>G	ENSP00000245407.3:n.1586+95C>G
ENST00000435065.6:c.1658+95C>G	ENSP00000402760.2:n.1658+95C>G
ENST00000447841.5:c.430+95C>G
ENST00000461013.5:n.9008+95C>G
ENST00000475308.1:n.2264+95C>G
NM_001308122.1:c.1658+95C>G	NP_001295051.1:n.1658+95C>G
NM_003060.3:c.1586+95C>G	NP_003051.1:n.1586+95C>G
XM_011543590.1:c.968+95C>G	XP_011541892.1:n.968+95C>G
XR_948290.1:n.1712+95C>G
XM_011543590.2:c.968+95C>G	XP_011541892.1:n.968+95C>G
XM_017009778.2:c.1058+95C>G	XP_016865267.1:n.1058+95C>G
XR_001742215.1:n.1841+95C>G
XR_001742216.1:n.1860+95C>G
XR_427718.2:n.1946+95C>G
XR_948290.2:n.1712+95C>G
XR_948291.2:n.1940+95C>G
NM_003060.4:c.1586+95C>G MANE Select	NP_003051.1:n.1586+95C>G
NM_001308122.2:c.1658+95C>G	NP_001295051.1:n.1658+95C>G