Canonical Allele Identifier: CA1583144745

Gene: SLC22A5

Linked Data

• dbSNP Id: rs1752796757
• gnomAD v4: 5-132394072-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132394074_132394075del , CM000667.2:g.132394074_132394075del	GRCh38
NC_000005.9:g.131729766_131729767del , CM000667.1:g.131729766_131729767del	GRCh37
NC_000005.8:g.131757665_131757666del	NCBI36
NG_008982.1:g.29366_29367del
NG_008982.2:g.29371_29372del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-111_1292-110del	ENSP00000388838.2:n.1292-111_1292-110del
ENST00000435065.7:c.1659-111_1659-110del	ENSP00000402760.2:n.1659-111_1659-110del
ENST00000448810.6:c.*439-111_*439-110del	ENSP00000401860.2:n.*439-111_*439-110del
ENST00000685543.1:n.1728-111_1728-110del
ENST00000686757.1:c.*751-111_*751-110del	ENSP00000510721.1:n.*751-111_*751-110del
ENST00000686868.1:n.579-111_579-110del
ENST00000687740.1:n.4272-111_4272-110del
ENST00000688151.1:n.2897-111_2897-110del
ENST00000689271.1:c.1434-111_1434-110del	ENSP00000510797.1:n.1434-111_1434-110del
ENST00000690900.1:c.*751-111_*751-110del	ENSP00000510703.1:n.*751-111_*751-110del
ENST00000692212.1:n.4727-111_4727-110del
ENST00000692355.1:c.840-111_840-110del
ENST00000692413.1:c.1569-111_1569-110del	ENSP00000509374.1:n.1569-111_1569-110del
ENST00000692825.1:c.1655-111_1655-110del	ENSP00000509447.1:n.1655-111_1655-110del
ENST00000693308.1:c.1635-111_1635-110del	ENSP00000509770.1:n.1635-111_1635-110del
ENST00000693763.1:n.2747-111_2747-110del
ENST00000245407.8:c.1587-111_1587-110del MANE Select	ENSP00000245407.3:n.1587-111_1587-110del
ENST00000245407.7:c.1587-111_1587-110del	ENSP00000245407.3:n.1587-111_1587-110del
ENST00000435065.6:c.1659-111_1659-110del	ENSP00000402760.2:n.1659-111_1659-110del
ENST00000447841.5:c.431-111_431-110del
ENST00000461013.5:n.9009-111_9009-110del
ENST00000475308.1:n.2265-111_2265-110del
NM_001308122.1:c.1659-111_1659-110del	NP_001295051.1:n.1659-111_1659-110del
NM_003060.3:c.1587-111_1587-110del	NP_003051.1:n.1587-111_1587-110del
XM_011543590.1:c.969-111_969-110del	XP_011541892.1:n.969-111_969-110del
XR_948290.1:n.1713-111_1713-110del
XM_011543590.2:c.969-111_969-110del	XP_011541892.1:n.969-111_969-110del
XM_017009778.2:c.1059-111_1059-110del	XP_016865267.1:n.1059-111_1059-110del
XR_001742215.1:n.1842-111_1842-110del
XR_001742216.1:n.1861-111_1861-110del
XR_427718.2:n.1947-111_1947-110del
XR_948290.2:n.1713-111_1713-110del
XR_948291.2:n.1941-111_1941-110del
NM_003060.4:c.1587-111_1587-110del MANE Select	NP_003051.1:n.1587-111_1587-110del
NM_001308122.2:c.1659-111_1659-110del	NP_001295051.1:n.1659-111_1659-110del