Canonical Allele Identifier: CA1583144514

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132385275_132385279delinsTAAGG , CM000667.2:g.132385275_132385279delinsTAAGG	GRCh38
NC_000005.9:g.131720967_131720971delinsTAAGG , CM000667.1:g.131720967_131720971delinsTAAGG	GRCh37
NC_000005.8:g.131748866_131748870delinsTAAGG	NCBI36
NG_008982.1:g.20567_20571delinsTAAGG
NG_008982.2:g.20572_20576delinsTAAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000415928.6:c.665+961_665+965delinsTAAGG	ENSP00000388838.2:n.665+961_665+965delins...
ENST00000435065.7:c.725-53_725-49delinsTAAGG	ENSP00000402760.2:n.725-53_725-49delinsTA...
ENST00000448810.6:c.653-53_653-49delinsTAAGG	ENSP00000401860.2:n.653-53_653-49delinsTA...
ENST00000686757.1:c.672-53_672-49delinsTAAGG	ENSP00000510721.1:n.672-53_672-49delinsTA...
ENST00000687740.1:n.1760_1764delinsTAAGG
ENST00000688151.1:n.1845-53_1845-49delinsTAAGG
ENST00000689271.1:c.671+955_671+959delinsTAAGG	ENSP00000510797.1:n.671+955_671+959delins...
ENST00000690900.1:c.672-101_672-97delinsTAAGG	ENSP00000510703.1:n.672-101_672-97delinsT...
ENST00000692212.1:n.426_430delinsTAAGG
ENST00000692355.1:c.204+974_204+978delinsTAAGG
ENST00000692413.1:c.672-53_672-49delinsTAAGG	ENSP00000509374.1:n.672-53_672-49delinsTA...
ENST00000692825.1:c.721-53_721-49delinsTAAGG	ENSP00000509447.1:n.721-53_721-49delinsTA...
ENST00000693308.1:c.666-53_666-49delinsTAAGG	ENSP00000509770.1:n.666-53_666-49delinsTA...
ENST00000693763.1:n.1760_1764delinsTAAGG
ENST00000245407.8:c.653-53_653-49delinsTAAGG MANE Select	ENSP00000245407.3:n.653-53_653-49delinsTA...
ENST00000245407.7:c.653-53_653-49delinsTAAGG	ENSP00000245407.3:n.653-53_653-49delinsTA...
ENST00000415928.5:c.422-53_422-49delinsTAAGG	ENSP00000388838.1:n.422-53_422-49delinsTA...
ENST00000435065.6:c.725-53_725-49delinsTAAGG	ENSP00000402760.2:n.725-53_725-49delinsTA...
ENST00000437841.6:c.394-53_394-49delinsTAAGG	ENSP00000400553.1:n.394-53_394-49delinsTA...
ENST00000461013.5:n.8075-53_8075-49delinsTAAGG
NM_001308122.1:c.725-53_725-49delinsTAAGG	NP_001295051.1:n.725-53_725-49delinsTAAGG...
NM_003060.3:c.653-53_653-49delinsTAAGG	NP_003051.1:n.653-53_653-49delinsTAAGG
XM_011543590.1:c.35-53_35-49delinsTAAGG	XP_011541892.1:n.35-53_35-49delinsTAAGG
XR_427718.1:n.1013-53_1013-49delinsTAAGG
XR_948290.1:n.994-53_994-49delinsTAAGG
XR_948291.1:n.1007-53_1007-49delinsTAAGG
XM_011543590.2:c.35-53_35-49delinsTAAGG	XP_011541892.1:n.35-53_35-49delinsTAAGG
XM_017009778.2:c.125-53_125-49delinsTAAGG	XP_016865267.1:n.125-53_125-49delinsTAAGG...
XR_001742215.1:n.994-53_994-49delinsTAAGG
XR_001742216.1:n.1013-53_1013-49delinsTAAGG
XR_427718.2:n.1013-53_1013-49delinsTAAGG
XR_948290.2:n.994-53_994-49delinsTAAGG
XR_948291.2:n.1007-53_1007-49delinsTAAGG
NM_003060.4:c.653-53_653-49delinsTAAGG MANE Select	NP_003051.1:n.653-53_653-49delinsTAAGG
NM_001308122.2:c.725-53_725-49delinsTAAGG	NP_001295051.1:n.725-53_725-49delinsTAAGG...