Canonical Allele Identifier: CA1583144483

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385215_132385219delinsTAGAG , CM000667.2:g.132385215_132385219delinsTAGAG	GRCh38
NC_000005.9:g.131720907_131720911delinsTAGAG , CM000667.1:g.131720907_131720911delinsTAGAG	GRCh37
NC_000005.8:g.131748806_131748810delinsTAGAG	NCBI36
NG_008982.1:g.20507_20511delinsTAGAG
NG_008982.2:g.20512_20516delinsTAGAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+901_665+905delinsTAGAG	ENSP00000388838.2:n.665+901_665+905delinsTAGAG
ENST00000435065.7:c.725-113_725-109delinsTAGAG	ENSP00000402760.2:n.725-113_725-109delinsTAGAG
ENST00000448810.6:c.653-113_653-109delinsTAGAG	ENSP00000401860.2:n.653-113_653-109delinsTAGAG
ENST00000686757.1:c.672-113_672-109delinsTAGAG	ENSP00000510721.1:n.672-113_672-109delinsTAGAG
ENST00000687740.1:n.1700_1704delinsTAGAG
ENST00000688151.1:n.1845-113_1845-109delinsTAGAG
ENST00000689271.1:c.671+895_671+899delinsTAGAG	ENSP00000510797.1:n.671+895_671+899delinsTAGAG
ENST00000690900.1:c.672-161_672-157delinsTAGAG	ENSP00000510703.1:n.672-161_672-157delinsTAGAG
ENST00000692212.1:n.366_370delinsTAGAG
ENST00000692355.1:c.204+914_204+918delinsTAGAG
ENST00000692413.1:c.672-113_672-109delinsTAGAG	ENSP00000509374.1:n.672-113_672-109delinsTAGAG
ENST00000692825.1:c.721-113_721-109delinsTAGAG	ENSP00000509447.1:n.721-113_721-109delinsTAGAG
ENST00000693308.1:c.666-113_666-109delinsTAGAG	ENSP00000509770.1:n.666-113_666-109delinsTAGAG
ENST00000693763.1:n.1700_1704delinsTAGAG
ENST00000245407.8:c.653-113_653-109delinsTAGAG MANE Select	ENSP00000245407.3:n.653-113_653-109delinsTAGAG
ENST00000245407.7:c.653-113_653-109delinsTAGAG	ENSP00000245407.3:n.653-113_653-109delinsTAGAG
ENST00000415928.5:c.422-113_422-109delinsTAGAG	ENSP00000388838.1:n.422-113_422-109delinsTAGAG
ENST00000435065.6:c.725-113_725-109delinsTAGAG	ENSP00000402760.2:n.725-113_725-109delinsTAGAG
ENST00000437841.6:c.394-113_394-109delinsTAGAG	ENSP00000400553.1:n.394-113_394-109delinsTAGAG
ENST00000461013.5:n.8075-113_8075-109delinsTAGAG
NM_001308122.1:c.725-113_725-109delinsTAGAG	NP_001295051.1:n.725-113_725-109delinsTAGAG
NM_003060.3:c.653-113_653-109delinsTAGAG	NP_003051.1:n.653-113_653-109delinsTAGAG
XM_011543590.1:c.35-113_35-109delinsTAGAG	XP_011541892.1:n.35-113_35-109delinsTAGAG
XR_427718.1:n.1013-113_1013-109delinsTAGAG
XR_948290.1:n.994-113_994-109delinsTAGAG
XR_948291.1:n.1007-113_1007-109delinsTAGAG
XM_011543590.2:c.35-113_35-109delinsTAGAG	XP_011541892.1:n.35-113_35-109delinsTAGAG
XM_017009778.2:c.125-113_125-109delinsTAGAG	XP_016865267.1:n.125-113_125-109delinsTAGAG
XR_001742215.1:n.994-113_994-109delinsTAGAG
XR_001742216.1:n.1013-113_1013-109delinsTAGAG
XR_427718.2:n.1013-113_1013-109delinsTAGAG
XR_948290.2:n.994-113_994-109delinsTAGAG
XR_948291.2:n.1007-113_1007-109delinsTAGAG
NM_003060.4:c.653-113_653-109delinsTAGAG MANE Select	NP_003051.1:n.653-113_653-109delinsTAGAG
NM_001308122.2:c.725-113_725-109delinsTAGAG	NP_001295051.1:n.725-113_725-109delinsTAGAG