Canonical Allele Identifier: CA1583144696

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1752793483

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393990_132393993del , CM000667.2:g.132393990_132393993del	GRCh38
NC_000005.9:g.131729682_131729685del , CM000667.1:g.131729682_131729685del	GRCh37
NC_000005.8:g.131757581_131757584del	NCBI36
NG_008982.1:g.29282_29285del
NG_008982.2:g.29287_29290del

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.1292-195_1292-192del	ENSP00000388838.2:n.1292-195_1292-192del
ENST00000435065.7:c.1658+179_1658+182del	ENSP00000402760.2:n.1658+179_1658+182del
ENST00000448810.6:c.*438+179_*438+182del	ENSP00000401860.2:n.*438+179_*438+182del
ENST00000685543.1:n.1727+179_1727+182del
ENST00000686757.1:c.*750+179_*750+182del	ENSP00000510721.1:n.*750+179_*750+182del
ENST00000686868.1:n.578+179_578+182del
ENST00000687740.1:n.4271+179_4271+182del
ENST00000688151.1:n.2896+179_2896+182del
ENST00000689271.1:c.1433+179_1433+182del	ENSP00000510797.1:n.1433+179_1433+182del
ENST00000690900.1:c.*750+179_*750+182del	ENSP00000510703.1:n.*750+179_*750+182del
ENST00000692212.1:n.4726+179_4726+182del
ENST00000692355.1:c.839+179_839+182del
ENST00000692413.1:c.1568+179_1568+182del	ENSP00000509374.1:n.1568+179_1568+182del
ENST00000692825.1:c.1654+179_1654+182del	ENSP00000509447.1:n.1654+179_1654+182del
ENST00000693308.1:c.1634+179_1634+182del	ENSP00000509770.1:n.1634+179_1634+182del
ENST00000693763.1:n.2746+179_2746+182del
ENST00000245407.8:c.1586+179_1586+182del MANE Select	ENSP00000245407.3:n.1586+179_1586+182del
ENST00000245407.7:c.1586+179_1586+182del	ENSP00000245407.3:n.1586+179_1586+182del
ENST00000435065.6:c.1658+179_1658+182del	ENSP00000402760.2:n.1658+179_1658+182del
ENST00000447841.5:c.430+179_430+182del
ENST00000461013.5:n.9008+179_9008+182del
ENST00000475308.1:n.2264+179_2264+182del
NM_001308122.1:c.1658+179_1658+182del	NP_001295051.1:n.1658+179_1658+182del
NM_003060.3:c.1586+179_1586+182del	NP_003051.1:n.1586+179_1586+182del
XM_011543590.1:c.968+179_968+182del	XP_011541892.1:n.968+179_968+182del
XR_948290.1:n.1712+179_1712+182del
XM_011543590.2:c.968+179_968+182del	XP_011541892.1:n.968+179_968+182del
XM_017009778.2:c.1058+179_1058+182del	XP_016865267.1:n.1058+179_1058+182del
XR_001742215.1:n.1841+179_1841+182del
XR_001742216.1:n.1860+179_1860+182del
XR_427718.2:n.1946+179_1946+182del
XR_948290.2:n.1712+179_1712+182del
XR_948291.2:n.1940+179_1940+182del
NM_003060.4:c.1586+179_1586+182del MANE Select	NP_003051.1:n.1586+179_1586+182del
NM_001308122.2:c.1658+179_1658+182del	NP_001295051.1:n.1658+179_1658+182del