Canonical Allele Identifier: CA127213164

Gene: SLC22A5

Linked Data

• dbSNP Id: rs562051092
• gnomAD v3: 5-132393947-A-G
• gnomAD v4: 5-132393947-A-G
• MyVariant Identifiers: chr5:g.131729639A>G (hg19) ; chr5:g.132393947A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393947A>G , CM000667.2:g.132393947A>G	GRCh38
NC_000005.9:g.131729639A>G , CM000667.1:g.131729639A>G	GRCh37
NC_000005.8:g.131757538A>G	NCBI36
NG_008982.1:g.29239A>G
NG_008982.2:g.29244A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-238A>G	ENSP00000388838.2:n.1292-238A>G
ENST00000435065.7:c.1658+136A>G	ENSP00000402760.2:n.1658+136A>G
ENST00000448810.6:c.*438+136A>G	ENSP00000401860.2:n.*438+136A>G
ENST00000685543.1:n.1727+136A>G
ENST00000686757.1:c.*750+136A>G	ENSP00000510721.1:n.*750+136A>G
ENST00000686868.1:n.578+136A>G
ENST00000687740.1:n.4271+136A>G
ENST00000688151.1:n.2896+136A>G
ENST00000689271.1:c.1433+136A>G	ENSP00000510797.1:n.1433+136A>G
ENST00000690900.1:c.*750+136A>G	ENSP00000510703.1:n.*750+136A>G
ENST00000692212.1:n.4726+136A>G
ENST00000692355.1:c.839+136A>G
ENST00000692413.1:c.1568+136A>G	ENSP00000509374.1:n.1568+136A>G
ENST00000692825.1:c.1654+136A>G	ENSP00000509447.1:n.1654+136A>G
ENST00000693308.1:c.1634+136A>G	ENSP00000509770.1:n.1634+136A>G
ENST00000693763.1:n.2746+136A>G
ENST00000245407.8:c.1586+136A>G MANE Select	ENSP00000245407.3:n.1586+136A>G
ENST00000245407.7:c.1586+136A>G	ENSP00000245407.3:n.1586+136A>G
ENST00000435065.6:c.1658+136A>G	ENSP00000402760.2:n.1658+136A>G
ENST00000447841.5:c.430+136A>G
ENST00000461013.5:n.9008+136A>G
ENST00000475308.1:n.2264+136A>G
NM_001308122.1:c.1658+136A>G	NP_001295051.1:n.1658+136A>G
NM_003060.3:c.1586+136A>G	NP_003051.1:n.1586+136A>G
XM_011543590.1:c.968+136A>G	XP_011541892.1:n.968+136A>G
XR_948290.1:n.1712+136A>G
XM_011543590.2:c.968+136A>G	XP_011541892.1:n.968+136A>G
XM_017009778.2:c.1058+136A>G	XP_016865267.1:n.1058+136A>G
XR_001742215.1:n.1841+136A>G
XR_001742216.1:n.1860+136A>G
XR_427718.2:n.1946+136A>G
XR_948290.2:n.1712+136A>G
XR_948291.2:n.1940+136A>G
NM_003060.4:c.1586+136A>G MANE Select	NP_003051.1:n.1586+136A>G
NM_001308122.2:c.1658+136A>G	NP_001295051.1:n.1658+136A>G