Canonical Allele Identifier: CA2562497524

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393460_132393469del , CM000667.2:g.132393460_132393469del	GRCh38
NC_000005.9:g.131729152_131729161del , CM000667.1:g.131729152_131729161del	GRCh37
NC_000005.8:g.131757051_131757060del	NCBI36
NG_008982.1:g.28752_28761del
NG_008982.2:g.28757_28766del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-725_1292-716del	ENSP00000388838.2:n.1292-725_1292-716del
ENST00000435065.7:c.1523-216_1523-207del	ENSP00000402760.2:n.1523-216_1523-207del
ENST00000448810.6:c.*303-216_*303-207del	ENSP00000401860.2:n.*303-216_*303-207del
ENST00000685543.1:n.1592-216_1592-207del
ENST00000686757.1:c.*615-216_*615-207del	ENSP00000510721.1:n.*615-216_*615-207del
ENST00000686868.1:n.227_236del
ENST00000687740.1:n.4136-216_4136-207del
ENST00000688151.1:n.2761-216_2761-207del
ENST00000689271.1:c.1298-216_1298-207del	ENSP00000510797.1:n.1298-216_1298-207del
ENST00000690900.1:c.*615-216_*615-207del	ENSP00000510703.1:n.*615-216_*615-207del
ENST00000692212.1:n.4591-216_4591-207del
ENST00000692355.1:c.704-216_704-207del
ENST00000692413.1:c.1433-216_1433-207del	ENSP00000509374.1:n.1433-216_1433-207del
ENST00000692825.1:c.1519-216_1519-207del	ENSP00000509447.1:n.1519-216_1519-207del
ENST00000693308.1:c.1499-216_1499-207del	ENSP00000509770.1:n.1499-216_1499-207del
ENST00000693763.1:n.2611-216_2611-207del
ENST00000245407.8:c.1451-216_1451-207del MANE Select	ENSP00000245407.3:n.1451-216_1451-207del
ENST00000245407.7:c.1451-216_1451-207del	ENSP00000245407.3:n.1451-216_1451-207del
ENST00000435065.6:c.1523-216_1523-207del	ENSP00000402760.2:n.1523-216_1523-207del
ENST00000447841.5:c.295-216_295-207del
ENST00000448810.5:c.713-216_713-207del
ENST00000461013.5:n.8873-216_8873-207del
ENST00000475308.1:n.2129-216_2129-207del
ENST00000479605.5:n.554-216_554-207del
NM_001308122.1:c.1523-216_1523-207del	NP_001295051.1:n.1523-216_1523-207del
NM_003060.3:c.1451-216_1451-207del	NP_003051.1:n.1451-216_1451-207del
XM_011543590.1:c.833-216_833-207del	XP_011541892.1:n.833-216_833-207del
XR_948290.1:n.1577-216_1577-207del
XM_011543590.2:c.833-216_833-207del	XP_011541892.1:n.833-216_833-207del
XM_017009778.2:c.923-216_923-207del	XP_016865267.1:n.923-216_923-207del
XR_001742215.1:n.1706-216_1706-207del
XR_001742216.1:n.1725-216_1725-207del
XR_427718.2:n.1811-216_1811-207del
XR_948290.2:n.1577-216_1577-207del
XR_948291.2:n.1805-216_1805-207del
NM_003060.4:c.1451-216_1451-207del MANE Select	NP_003051.1:n.1451-216_1451-207del
NM_001308122.2:c.1523-216_1523-207del	NP_001295051.1:n.1523-216_1523-207del