Canonical Allele Identifier: CA1583144755

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1752797964

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132394103_132394104insGTGT , CM000667.2:g.132394103_132394104insGTGT	GRCh38
NC_000005.9:g.131729795_131729796insGTGT , CM000667.1:g.131729795_131729796insGTGT	GRCh37
NC_000005.8:g.131757694_131757695insGTGT	NCBI36
NG_008982.1:g.29395_29396insGTGT
NG_008982.2:g.29400_29401insGTGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1292-82_1292-81insGTGT	ENSP00000388838.2:n.1292-82_1292-81insGTG...
ENST00000435065.7:c.1659-82_1659-81insGTGT	ENSP00000402760.2:n.1659-82_1659-81insGTG...
ENST00000448810.6:c.*439-82_*439-81insGTGT	ENSP00000401860.2:n.*439-82_*439-81insGTG...
ENST00000685543.1:n.1728-82_1728-81insGTGT
ENST00000686757.1:c.*751-82_*751-81insGTGT	ENSP00000510721.1:n.*751-82_*751-81insGTG...
ENST00000686868.1:n.579-82_579-81insGTGT
ENST00000687740.1:n.4272-82_4272-81insGTGT
ENST00000688151.1:n.2897-82_2897-81insGTGT
ENST00000689271.1:c.1434-82_1434-81insGTGT	ENSP00000510797.1:n.1434-82_1434-81insGTG...
ENST00000690900.1:c.*751-82_*751-81insGTGT	ENSP00000510703.1:n.*751-82_*751-81insGTG...
ENST00000692212.1:n.4727-82_4727-81insGTGT
ENST00000692355.1:c.840-82_840-81insGTGT
ENST00000692413.1:c.1569-82_1569-81insGTGT	ENSP00000509374.1:n.1569-82_1569-81insGTG...
ENST00000692825.1:c.1655-82_1655-81insGTGT	ENSP00000509447.1:n.1655-82_1655-81insGTG...
ENST00000693308.1:c.1635-82_1635-81insGTGT	ENSP00000509770.1:n.1635-82_1635-81insGTG...
ENST00000693763.1:n.2747-82_2747-81insGTGT
ENST00000245407.8:c.1587-82_1587-81insGTGT MANE Select	ENSP00000245407.3:n.1587-82_1587-81insGTG...
ENST00000245407.7:c.1587-82_1587-81insGTGT	ENSP00000245407.3:n.1587-82_1587-81insGTG...
ENST00000435065.6:c.1659-82_1659-81insGTGT	ENSP00000402760.2:n.1659-82_1659-81insGTG...
ENST00000447841.5:c.431-82_431-81insGTGT
ENST00000461013.5:n.9009-82_9009-81insGTGT
ENST00000475308.1:n.2265-82_2265-81insGTGT
NM_001308122.1:c.1659-82_1659-81insGTGT	NP_001295051.1:n.1659-82_1659-81insGTGT
NM_003060.3:c.1587-82_1587-81insGTGT	NP_003051.1:n.1587-82_1587-81insGTGT
XM_011543590.1:c.969-82_969-81insGTGT	XP_011541892.1:n.969-82_969-81insGTGT
XR_948290.1:n.1713-82_1713-81insGTGT
XM_011543590.2:c.969-82_969-81insGTGT	XP_011541892.1:n.969-82_969-81insGTGT
XM_017009778.2:c.1059-82_1059-81insGTGT	XP_016865267.1:n.1059-82_1059-81insGTGT
XR_001742215.1:n.1842-82_1842-81insGTGT
XR_001742216.1:n.1861-82_1861-81insGTGT
XR_427718.2:n.1947-82_1947-81insGTGT
XR_948290.2:n.1713-82_1713-81insGTGT
XR_948291.2:n.1941-82_1941-81insGTGT
NM_003060.4:c.1587-82_1587-81insGTGT MANE Select	NP_003051.1:n.1587-82_1587-81insGTGT
NM_001308122.2:c.1659-82_1659-81insGTGT	NP_001295051.1:n.1659-82_1659-81insGTGT