Canonical Allele Identifier: CA1583144299

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393592_132393601delinsAGAGTCCTGG , CM000667.2:g.132393592_132393601delinsAGAGTCCTGG	GRCh38
NC_000005.9:g.131729284_131729293delinsAGAGTCCTGG , CM000667.1:g.131729284_131729293delinsAGAGTCCTGG	GRCh37
NC_000005.8:g.131757183_131757192delinsAGAGTCCTGG	NCBI36
NG_008982.1:g.28884_28893delinsAGAGTCCTGG
NG_008982.2:g.28889_28898delinsAGAGTCCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-593_1292-584delinsAGAGTCCTGG	ENSP00000388838.2:n.1292-593_1292-584delinsAGAGTCCTGG
ENST00000435065.7:c.1523-84_1523-75delinsAGAGTCCTGG	ENSP00000402760.2:n.1523-84_1523-75delinsAGAGTCCTGG
ENST00000448810.6:c.*303-84_*303-75delinsAGAGTCCTGG	ENSP00000401860.2:n.*303-84_*303-75delinsAGAGTCCTGG
ENST00000685543.1:n.1592-84_1592-75delinsAGAGTCCTGG
ENST00000686757.1:c.*615-84_*615-75delinsAGAGTCCTGG	ENSP00000510721.1:n.*615-84_*615-75delinsAGAGTCCTGG
ENST00000686868.1:n.359_368delinsAGAGTCCTGG
ENST00000687740.1:n.4136-84_4136-75delinsAGAGTCCTGG
ENST00000688151.1:n.2761-84_2761-75delinsAGAGTCCTGG
ENST00000689271.1:c.1298-84_1298-75delinsAGAGTCCTGG	ENSP00000510797.1:n.1298-84_1298-75delinsAGAGTCCTGG
ENST00000690900.1:c.*615-84_*615-75delinsAGAGTCCTGG	ENSP00000510703.1:n.*615-84_*615-75delinsAGAGTCCTGG
ENST00000692212.1:n.4591-84_4591-75delinsAGAGTCCTGG
ENST00000692355.1:c.704-84_704-75delinsAGAGTCCTGG
ENST00000692413.1:c.1433-84_1433-75delinsAGAGTCCTGG	ENSP00000509374.1:n.1433-84_1433-75delinsAGAGTCCTGG
ENST00000692825.1:c.1519-84_1519-75delinsAGAGTCCTGG	ENSP00000509447.1:n.1519-84_1519-75delinsAGAGTCCTGG
ENST00000693308.1:c.1499-84_1499-75delinsAGAGTCCTGG	ENSP00000509770.1:n.1499-84_1499-75delinsAGAGTCCTGG
ENST00000693763.1:n.2611-84_2611-75delinsAGAGTCCTGG
ENST00000245407.8:c.1451-84_1451-75delinsAGAGTCCTGG MANE Select	ENSP00000245407.3:n.1451-84_1451-75delinsAGAGTCCTGG
ENST00000245407.7:c.1451-84_1451-75delinsAGAGTCCTGG	ENSP00000245407.3:n.1451-84_1451-75delinsAGAGTCCTGG
ENST00000435065.6:c.1523-84_1523-75delinsAGAGTCCTGG	ENSP00000402760.2:n.1523-84_1523-75delinsAGAGTCCTGG
ENST00000447841.5:c.295-84_295-75delinsAGAGTCCTGG
ENST00000448810.5:c.713-84_713-75delinsAGAGTCCTGG
ENST00000461013.5:n.8873-84_8873-75delinsAGAGTCCTGG
ENST00000475308.1:n.2129-84_2129-75delinsAGAGTCCTGG
ENST00000479605.5:n.554-84_554-75delinsAGAGTCCTGG
NM_001308122.1:c.1523-84_1523-75delinsAGAGTCCTGG	NP_001295051.1:n.1523-84_1523-75delinsAGAGTCCTGG
NM_003060.3:c.1451-84_1451-75delinsAGAGTCCTGG	NP_003051.1:n.1451-84_1451-75delinsAGAGTCCTGG
XM_011543590.1:c.833-84_833-75delinsAGAGTCCTGG	XP_011541892.1:n.833-84_833-75delinsAGAGTCCTGG
XR_948290.1:n.1577-84_1577-75delinsAGAGTCCTGG
XM_011543590.2:c.833-84_833-75delinsAGAGTCCTGG	XP_011541892.1:n.833-84_833-75delinsAGAGTCCTGG
XM_017009778.2:c.923-84_923-75delinsAGAGTCCTGG	XP_016865267.1:n.923-84_923-75delinsAGAGTCCTGG
XR_001742215.1:n.1706-84_1706-75delinsAGAGTCCTGG
XR_001742216.1:n.1725-84_1725-75delinsAGAGTCCTGG
XR_427718.2:n.1811-84_1811-75delinsAGAGTCCTGG
XR_948290.2:n.1577-84_1577-75delinsAGAGTCCTGG
XR_948291.2:n.1805-84_1805-75delinsAGAGTCCTGG
NM_003060.4:c.1451-84_1451-75delinsAGAGTCCTGG MANE Select	NP_003051.1:n.1451-84_1451-75delinsAGAGTCCTGG
NM_001308122.2:c.1523-84_1523-75delinsAGAGTCCTGG	NP_001295051.1:n.1523-84_1523-75delinsAGAGTCCTGG