Canonical Allele Identifier: CA1583144392

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385012_132385013delinsGA , CM000667.2:g.132385012_132385013delinsGA	GRCh38
NC_000005.9:g.131720704_131720705delinsGA , CM000667.1:g.131720704_131720705delinsGA	GRCh37
NC_000005.8:g.131748603_131748604delinsGA	NCBI36
NG_008982.1:g.20304_20305delinsGA
NG_008982.2:g.20309_20310delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.665+698_665+699delinsGA	ENSP00000388838.2:n.665+698_665+699delinsGA
ENST00000435065.7:c.725-316_725-315delinsGA	ENSP00000402760.2:n.725-316_725-315delinsGA
ENST00000448810.6:c.653-316_653-315delinsGA	ENSP00000401860.2:n.653-316_653-315delinsGA
ENST00000686757.1:c.672-316_672-315delinsGA	ENSP00000510721.1:n.672-316_672-315delinsGA
ENST00000687740.1:n.1497_1498delinsGA
ENST00000688151.1:n.1845-316_1845-315delinsGA
ENST00000689271.1:c.671+692_671+693delinsGA	ENSP00000510797.1:n.671+692_671+693delinsGA
ENST00000690900.1:c.672-364_672-363delinsGA	ENSP00000510703.1:n.672-364_672-363delinsGA
ENST00000692212.1:n.163_164delinsGA
ENST00000692355.1:c.204+711_204+712delinsGA
ENST00000692413.1:c.672-316_672-315delinsGA	ENSP00000509374.1:n.672-316_672-315delinsGA
ENST00000692825.1:c.721-316_721-315delinsGA	ENSP00000509447.1:n.721-316_721-315delinsGA
ENST00000693308.1:c.666-316_666-315delinsGA	ENSP00000509770.1:n.666-316_666-315delinsGA
ENST00000693763.1:n.1497_1498delinsGA
ENST00000245407.8:c.653-316_653-315delinsGA MANE Select	ENSP00000245407.3:n.653-316_653-315delinsGA
ENST00000245407.7:c.653-316_653-315delinsGA	ENSP00000245407.3:n.653-316_653-315delinsGA
ENST00000415928.5:c.422-316_422-315delinsGA	ENSP00000388838.1:n.422-316_422-315delinsGA
ENST00000435065.6:c.725-316_725-315delinsGA	ENSP00000402760.2:n.725-316_725-315delinsGA
ENST00000437841.6:c.394-316_394-315delinsGA	ENSP00000400553.1:n.394-316_394-315delinsGA
ENST00000461013.5:n.8075-316_8075-315delinsGA
NM_001308122.1:c.725-316_725-315delinsGA	NP_001295051.1:n.725-316_725-315delinsGA
NM_003060.3:c.653-316_653-315delinsGA	NP_003051.1:n.653-316_653-315delinsGA
XM_011543590.1:c.35-316_35-315delinsGA	XP_011541892.1:n.35-316_35-315delinsGA
XR_427718.1:n.1013-316_1013-315delinsGA
XR_948290.1:n.994-316_994-315delinsGA
XR_948291.1:n.1007-316_1007-315delinsGA
XM_011543590.2:c.35-316_35-315delinsGA	XP_011541892.1:n.35-316_35-315delinsGA
XM_017009778.2:c.125-316_125-315delinsGA	XP_016865267.1:n.125-316_125-315delinsGA
XR_001742215.1:n.994-316_994-315delinsGA
XR_001742216.1:n.1013-316_1013-315delinsGA
XR_427718.2:n.1013-316_1013-315delinsGA
XR_948290.2:n.994-316_994-315delinsGA
XR_948291.2:n.1007-316_1007-315delinsGA
NM_003060.4:c.653-316_653-315delinsGA MANE Select	NP_003051.1:n.653-316_653-315delinsGA
NM_001308122.2:c.725-316_725-315delinsGA	NP_001295051.1:n.725-316_725-315delinsGA