Canonical Allele Identifier: CA2675199778

Gene: SLC22A5

Linked Data

• gnomAD v4: 5-132393860-CCAGGTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132393865_132393871del , CM000667.2:g.132393865_132393871del	GRCh38
NC_000005.9:g.131729557_131729563del , CM000667.1:g.131729557_131729563del	GRCh37
NC_000005.8:g.131757456_131757462del	NCBI36
NG_008982.1:g.29157_29163del
NG_008982.2:g.29162_29168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.1292-320_1292-314del	ENSP00000388838.2:n.1292-320_1292-314del
ENST00000435065.7:c.1658+54_1658+60del	ENSP00000402760.2:n.1658+54_1658+60del
ENST00000448810.6:c.*438+54_*438+60del	ENSP00000401860.2:n.*438+54_*438+60del
ENST00000685543.1:n.1727+54_1727+60del
ENST00000686757.1:c.*750+54_*750+60del	ENSP00000510721.1:n.*750+54_*750+60del
ENST00000686868.1:n.578+54_578+60del
ENST00000687740.1:n.4271+54_4271+60del
ENST00000688151.1:n.2896+54_2896+60del
ENST00000689271.1:c.1433+54_1433+60del	ENSP00000510797.1:n.1433+54_1433+60del
ENST00000690900.1:c.*750+54_*750+60del	ENSP00000510703.1:n.*750+54_*750+60del
ENST00000692212.1:n.4726+54_4726+60del
ENST00000692355.1:c.839+54_839+60del
ENST00000692413.1:c.1568+54_1568+60del	ENSP00000509374.1:n.1568+54_1568+60del
ENST00000692825.1:c.1654+54_1654+60del	ENSP00000509447.1:n.1654+54_1654+60del
ENST00000693308.1:c.1634+54_1634+60del	ENSP00000509770.1:n.1634+54_1634+60del
ENST00000693763.1:n.2746+54_2746+60del
ENST00000245407.8:c.1586+54_1586+60del MANE Select	ENSP00000245407.3:n.1586+54_1586+60del
ENST00000245407.7:c.1586+54_1586+60del	ENSP00000245407.3:n.1586+54_1586+60del
ENST00000435065.6:c.1658+54_1658+60del	ENSP00000402760.2:n.1658+54_1658+60del
ENST00000447841.5:c.430+54_430+60del
ENST00000461013.5:n.9008+54_9008+60del
ENST00000475308.1:n.2264+54_2264+60del
NM_001308122.1:c.1658+54_1658+60del	NP_001295051.1:n.1658+54_1658+60del
NM_003060.3:c.1586+54_1586+60del	NP_003051.1:n.1586+54_1586+60del
XM_011543590.1:c.968+54_968+60del	XP_011541892.1:n.968+54_968+60del
XR_948290.1:n.1712+54_1712+60del
XM_011543590.2:c.968+54_968+60del	XP_011541892.1:n.968+54_968+60del
XM_017009778.2:c.1058+54_1058+60del	XP_016865267.1:n.1058+54_1058+60del
XR_001742215.1:n.1841+54_1841+60del
XR_001742216.1:n.1860+54_1860+60del
XR_427718.2:n.1946+54_1946+60del
XR_948290.2:n.1712+54_1712+60del
XR_948291.2:n.1940+54_1940+60del
NM_003060.4:c.1586+54_1586+60del MANE Select	NP_003051.1:n.1586+54_1586+60del
NM_001308122.2:c.1658+54_1658+60del	NP_001295051.1:n.1658+54_1658+60del