Canonical Allele Identifier: CA2675203634

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132390441-TGCTGGGACAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390442_132390451del , CM000667.2:g.132390442_132390451del	GRCh38
NC_000005.9:g.131726134_131726143del , CM000667.1:g.131726134_131726143del	GRCh37
NC_000005.8:g.131754033_131754042del	NCBI36
NG_008982.1:g.25734_25743del
NG_008982.2:g.25739_25748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-248_894-239del	ENSP00000388838.2:n.894-248_894-239del
ENST00000435065.7:c.1125-248_1125-239del	ENSP00000402760.2:n.1125-248_1125-239del
ENST00000448810.6:c.1053-334_1053-325del	ENSP00000401860.2:n.1053-334_1053-325del
ENST00000685543.1:n.1194-248_1194-239del
ENST00000686757.1:c.*217-248_*217-239del	ENSP00000510721.1:n.*217-248_*217-239del
ENST00000687740.1:n.3738-248_3738-239del
ENST00000688151.1:n.2363-248_2363-239del
ENST00000689271.1:c.900-248_900-239del	ENSP00000510797.1:n.900-248_900-239del
ENST00000690900.1:c.*217-248_*217-239del	ENSP00000510703.1:n.*217-248_*217-239del
ENST00000692212.1:n.2417_2426del
ENST00000692355.1:c.306-248_306-239del
ENST00000692413.1:c.1035-248_1035-239del	ENSP00000509374.1:n.1035-248_1035-239del
ENST00000692825.1:c.1121-248_1121-239del	ENSP00000509447.1:n.1121-248_1121-239del
ENST00000693308.1:c.1101-248_1101-239del	ENSP00000509770.1:n.1101-248_1101-239del
ENST00000693763.1:n.2213-248_2213-239del
ENST00000245407.8:c.1053-248_1053-239del MANE Select	ENSP00000245407.3:n.1053-248_1053-239del
ENST00000245407.7:c.1053-248_1053-239del	ENSP00000245407.3:n.1053-248_1053-239del
ENST00000435065.6:c.1125-248_1125-239del	ENSP00000402760.2:n.1125-248_1125-239del
ENST00000447841.5:c.111+1421_111+1430del
ENST00000448810.5:c.401-334_401-325del
ENST00000461013.5:n.8475-248_8475-239del
ENST00000475308.1:n.1483_1492del
ENST00000479605.5:n.156-248_156-239del
NM_001308122.1:c.1125-248_1125-239del	NP_001295051.1:n.1125-248_1125-239del
NM_003060.3:c.1053-248_1053-239del	NP_003051.1:n.1053-248_1053-239del
XM_011543590.1:c.435-248_435-239del	XP_011541892.1:n.435-248_435-239del
XR_427718.1:n.1413-248_1413-239del
XR_948290.1:n.1393+1421_1393+1430del
XR_948291.1:n.1407-248_1407-239del
XM_011543590.2:c.435-248_435-239del	XP_011541892.1:n.435-248_435-239del
XM_017009778.2:c.525-248_525-239del	XP_016865267.1:n.525-248_525-239del
XR_001742215.1:n.1394-334_1394-325del
XR_001742216.1:n.1413-334_1413-325del
XR_427718.2:n.1413-248_1413-239del
XR_948290.2:n.1393+1421_1393+1430del
XR_948291.2:n.1407-248_1407-239del
NM_003060.4:c.1053-248_1053-239del MANE Select	NP_003051.1:n.1053-248_1053-239del
NM_001308122.2:c.1125-248_1125-239del	NP_001295051.1:n.1125-248_1125-239del