Canonical Allele Identifier: CA2566201038

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132390438_132390439insAAAAATCC , CM000667.2:g.132390438_132390439insAAAAATCC	GRCh38
NC_000005.9:g.131726130_131726131insAAAAATCC , CM000667.1:g.131726130_131726131insAAAAATCC	GRCh37
NC_000005.8:g.131754029_131754030insAAAAATCC	NCBI36
NG_008982.1:g.25730_25731insAAAAATCC
NG_008982.2:g.25735_25736insAAAAATCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.894-252_894-251insAAAAATCC	ENSP00000388838.2:n.894-252_894-251insAAAAATCC
ENST00000435065.7:c.1125-252_1125-251insAAAAATCC	ENSP00000402760.2:n.1125-252_1125-251insAAAAATCC
ENST00000448810.6:c.1053-338_1053-337insAAAAATCC	ENSP00000401860.2:n.1053-338_1053-337insAAAAATCC
ENST00000685543.1:n.1194-252_1194-251insAAAAATCC
ENST00000686757.1:c.*217-252_*217-251insAAAAATCC	ENSP00000510721.1:n.*217-252_*217-251insAAAAATCC
ENST00000687740.1:n.3738-252_3738-251insAAAAATCC
ENST00000688151.1:n.2363-252_2363-251insAAAAATCC
ENST00000689271.1:c.900-252_900-251insAAAAATCC	ENSP00000510797.1:n.900-252_900-251insAAAAATCC
ENST00000690900.1:c.*217-252_*217-251insAAAAATCC	ENSP00000510703.1:n.*217-252_*217-251insAAAAATCC
ENST00000692212.1:n.2413_2414insAAAAATCC
ENST00000692355.1:c.306-252_306-251insAAAAATCC
ENST00000692413.1:c.1035-252_1035-251insAAAAATCC	ENSP00000509374.1:n.1035-252_1035-251insAAAAATCC
ENST00000692825.1:c.1121-252_1121-251insAAAAATCC	ENSP00000509447.1:n.1121-252_1121-251insAAAAATCC
ENST00000693308.1:c.1101-252_1101-251insAAAAATCC	ENSP00000509770.1:n.1101-252_1101-251insAAAAATCC
ENST00000693763.1:n.2213-252_2213-251insAAAAATCC
ENST00000245407.8:c.1053-252_1053-251insAAAAATCC MANE Select	ENSP00000245407.3:n.1053-252_1053-251insAAAAATCC
ENST00000245407.7:c.1053-252_1053-251insAAAAATCC	ENSP00000245407.3:n.1053-252_1053-251insAAAAATCC
ENST00000435065.6:c.1125-252_1125-251insAAAAATCC	ENSP00000402760.2:n.1125-252_1125-251insAAAAATCC
ENST00000447841.5:c.111+1417_111+1418insAAAAATCC
ENST00000448810.5:c.401-338_401-337insAAAAATCC
ENST00000461013.5:n.8475-252_8475-251insAAAAATCC
ENST00000475308.1:n.1479_1480insAAAAATCC
ENST00000479605.5:n.156-252_156-251insAAAAATCC
NM_001308122.1:c.1125-252_1125-251insAAAAATCC	NP_001295051.1:n.1125-252_1125-251insAAAAATCC
NM_003060.3:c.1053-252_1053-251insAAAAATCC	NP_003051.1:n.1053-252_1053-251insAAAAATCC
XM_011543590.1:c.435-252_435-251insAAAAATCC	XP_011541892.1:n.435-252_435-251insAAAAATCC
XR_427718.1:n.1413-252_1413-251insAAAAATCC
XR_948290.1:n.1393+1417_1393+1418insAAAAATCC
XR_948291.1:n.1407-252_1407-251insAAAAATCC
XM_011543590.2:c.435-252_435-251insAAAAATCC	XP_011541892.1:n.435-252_435-251insAAAAATCC
XM_017009778.2:c.525-252_525-251insAAAAATCC	XP_016865267.1:n.525-252_525-251insAAAAATCC
XR_001742215.1:n.1394-338_1394-337insAAAAATCC
XR_001742216.1:n.1413-338_1413-337insAAAAATCC
XR_427718.2:n.1413-252_1413-251insAAAAATCC
XR_948290.2:n.1393+1417_1393+1418insAAAAATCC
XR_948291.2:n.1407-252_1407-251insAAAAATCC
NM_003060.4:c.1053-252_1053-251insAAAAATCC MANE Select	NP_003051.1:n.1053-252_1053-251insAAAAATCC
NM_001308122.2:c.1125-252_1125-251insAAAAATCC	NP_001295051.1:n.1125-252_1125-251insAAAAATCC