Canonical Allele Identifier: CA1583144692

Gene: SLC22A5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393988_132393992delinsGTTCC , CM000667.2:g.132393988_132393992delinsGTTCC	GRCh38
NC_000005.9:g.131729680_131729684delinsGTTCC , CM000667.1:g.131729680_131729684delinsGTTCC	GRCh37
NC_000005.8:g.131757579_131757583delinsGTTCC	NCBI36
NG_008982.1:g.29280_29284delinsGTTCC
NG_008982.2:g.29285_29289delinsGTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-197_1292-193delinsGTTCC	ENSP00000388838.2:n.1292-197_1292-193delinsGTTCC
ENST00000435065.7:c.1658+177_1658+181delinsGTTCC	ENSP00000402760.2:n.1658+177_1658+181delinsGTTCC
ENST00000448810.6:c.*438+177_*438+181delinsGTTCC	ENSP00000401860.2:n.*438+177_*438+181delinsGTTCC
ENST00000685543.1:n.1727+177_1727+181delinsGTTCC
ENST00000686757.1:c.*750+177_*750+181delinsGTTCC	ENSP00000510721.1:n.*750+177_*750+181delinsGTTCC
ENST00000686868.1:n.578+177_578+181delinsGTTCC
ENST00000687740.1:n.4271+177_4271+181delinsGTTCC
ENST00000688151.1:n.2896+177_2896+181delinsGTTCC
ENST00000689271.1:c.1433+177_1433+181delinsGTTCC	ENSP00000510797.1:n.1433+177_1433+181delinsGTTCC
ENST00000690900.1:c.*750+177_*750+181delinsGTTCC	ENSP00000510703.1:n.*750+177_*750+181delinsGTTCC
ENST00000692212.1:n.4726+177_4726+181delinsGTTCC
ENST00000692355.1:c.839+177_839+181delinsGTTCC
ENST00000692413.1:c.1568+177_1568+181delinsGTTCC	ENSP00000509374.1:n.1568+177_1568+181delinsGTTCC
ENST00000692825.1:c.1654+177_1654+181delinsGTTCC	ENSP00000509447.1:n.1654+177_1654+181delinsGTTCC
ENST00000693308.1:c.1634+177_1634+181delinsGTTCC	ENSP00000509770.1:n.1634+177_1634+181delinsGTTCC
ENST00000693763.1:n.2746+177_2746+181delinsGTTCC
ENST00000245407.8:c.1586+177_1586+181delinsGTTCC MANE Select	ENSP00000245407.3:n.1586+177_1586+181delinsGTTCC
ENST00000245407.7:c.1586+177_1586+181delinsGTTCC	ENSP00000245407.3:n.1586+177_1586+181delinsGTTCC
ENST00000435065.6:c.1658+177_1658+181delinsGTTCC	ENSP00000402760.2:n.1658+177_1658+181delinsGTTCC
ENST00000447841.5:c.430+177_430+181delinsGTTCC
ENST00000461013.5:n.9008+177_9008+181delinsGTTCC
ENST00000475308.1:n.2264+177_2264+181delinsGTTCC
NM_001308122.1:c.1658+177_1658+181delinsGTTCC	NP_001295051.1:n.1658+177_1658+181delinsGTTCC
NM_003060.3:c.1586+177_1586+181delinsGTTCC	NP_003051.1:n.1586+177_1586+181delinsGTTCC
XM_011543590.1:c.968+177_968+181delinsGTTCC	XP_011541892.1:n.968+177_968+181delinsGTTCC
XR_948290.1:n.1712+177_1712+181delinsGTTCC
XM_011543590.2:c.968+177_968+181delinsGTTCC	XP_011541892.1:n.968+177_968+181delinsGTTCC
XM_017009778.2:c.1058+177_1058+181delinsGTTCC	XP_016865267.1:n.1058+177_1058+181delinsGTTCC
XR_001742215.1:n.1841+177_1841+181delinsGTTCC
XR_001742216.1:n.1860+177_1860+181delinsGTTCC
XR_427718.2:n.1946+177_1946+181delinsGTTCC
XR_948290.2:n.1712+177_1712+181delinsGTTCC
XR_948291.2:n.1940+177_1940+181delinsGTTCC
NM_003060.4:c.1586+177_1586+181delinsGTTCC MANE Select	NP_003051.1:n.1586+177_1586+181delinsGTTCC
NM_001308122.2:c.1658+177_1658+181delinsGTTCC	NP_001295051.1:n.1658+177_1658+181delinsGTTCC