Canonical Allele Identifier: CA2768436486

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390452_132390453insTTTTTTT , CM000667.2:g.132390452_132390453insTTTTTTT	GRCh38
NC_000005.9:g.131726144_131726145insTTTTTTT , CM000667.1:g.131726144_131726145insTTTTTTT	GRCh37
NC_000005.8:g.131754043_131754044insTTTTTTT	NCBI36
NG_008982.1:g.25744_25745insTTTTTTT
NG_008982.2:g.25749_25750insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-238_894-237insTTTTTTT	ENSP00000388838.2:n.894-238_894-237insTTTTTTT
ENST00000435065.7:c.1125-238_1125-237insTTTTTTT	ENSP00000402760.2:n.1125-238_1125-237insTTTTTTT
ENST00000448810.6:c.1053-324_1053-323insTTTTTTT	ENSP00000401860.2:n.1053-324_1053-323insTTTTTTT
ENST00000685543.1:n.1194-238_1194-237insTTTTTTT
ENST00000686757.1:c.*217-238_*217-237insTTTTTTT	ENSP00000510721.1:n.*217-238_*217-237insTTTTTTT
ENST00000687740.1:n.3738-238_3738-237insTTTTTTT
ENST00000688151.1:n.2363-238_2363-237insTTTTTTT
ENST00000689271.1:c.900-238_900-237insTTTTTTT	ENSP00000510797.1:n.900-238_900-237insTTTTTTT
ENST00000690900.1:c.*217-238_*217-237insTTTTTTT	ENSP00000510703.1:n.*217-238_*217-237insTTTTTTT
ENST00000692212.1:n.2427_2428insTTTTTTT
ENST00000692355.1:c.306-238_306-237insTTTTTTT
ENST00000692413.1:c.1035-238_1035-237insTTTTTTT	ENSP00000509374.1:n.1035-238_1035-237insTTTTTTT
ENST00000692825.1:c.1121-238_1121-237insTTTTTTT	ENSP00000509447.1:n.1121-238_1121-237insTTTTTTT
ENST00000693308.1:c.1101-238_1101-237insTTTTTTT	ENSP00000509770.1:n.1101-238_1101-237insTTTTTTT
ENST00000693763.1:n.2213-238_2213-237insTTTTTTT
ENST00000245407.8:c.1053-238_1053-237insTTTTTTT MANE Select	ENSP00000245407.3:n.1053-238_1053-237insTTTTTTT
ENST00000245407.7:c.1053-238_1053-237insTTTTTTT	ENSP00000245407.3:n.1053-238_1053-237insTTTTTTT
ENST00000435065.6:c.1125-238_1125-237insTTTTTTT	ENSP00000402760.2:n.1125-238_1125-237insTTTTTTT
ENST00000447841.5:c.111+1431_111+1432insTTTTTTT
ENST00000448810.5:c.401-324_401-323insTTTTTTT
ENST00000461013.5:n.8475-238_8475-237insTTTTTTT
ENST00000475308.1:n.1493_1494insTTTTTTT
ENST00000479605.5:n.156-238_156-237insTTTTTTT
NM_001308122.1:c.1125-238_1125-237insTTTTTTT	NP_001295051.1:n.1125-238_1125-237insTTTTTTT
NM_003060.3:c.1053-238_1053-237insTTTTTTT	NP_003051.1:n.1053-238_1053-237insTTTTTTT
XM_011543590.1:c.435-238_435-237insTTTTTTT	XP_011541892.1:n.435-238_435-237insTTTTTTT
XR_427718.1:n.1413-238_1413-237insTTTTTTT
XR_948290.1:n.1393+1431_1393+1432insTTTTTTT
XR_948291.1:n.1407-238_1407-237insTTTTTTT
XM_011543590.2:c.435-238_435-237insTTTTTTT	XP_011541892.1:n.435-238_435-237insTTTTTTT
XM_017009778.2:c.525-238_525-237insTTTTTTT	XP_016865267.1:n.525-238_525-237insTTTTTTT
XR_001742215.1:n.1394-324_1394-323insTTTTTTT
XR_001742216.1:n.1413-324_1413-323insTTTTTTT
XR_427718.2:n.1413-238_1413-237insTTTTTTT
XR_948290.2:n.1393+1431_1393+1432insTTTTTTT
XR_948291.2:n.1407-238_1407-237insTTTTTTT
NM_003060.4:c.1053-238_1053-237insTTTTTTT MANE Select	NP_003051.1:n.1053-238_1053-237insTTTTTTT
NM_001308122.2:c.1125-238_1125-237insTTTTTTT	NP_001295051.1:n.1125-238_1125-237insTTTTTTT