Canonical Allele Identifier: CA2675195203

Gene: SLC22A5 MIR3936HG

Linked Data

• gnomAD v4: 5-132369850-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369851_132369852del , CM000667.2:g.132369851_132369852del	GRCh38
NC_000005.9:g.131705543_131705544del , CM000667.1:g.131705543_131705544del	GRCh37
NC_000005.8:g.131733442_131733443del	NCBI36
NG_008982.1:g.5143_5144del
NG_008982.2:g.5148_5149del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.-122_-121del (SLC22A5)	ENSP00000388838.2:n.-122_-121del
ENST00000435065.7:c.-122_-121del (SLC22A5)	ENSP00000402760.2:n.-122_-121del
ENST00000448810.6:c.-122_-121del (SLC22A5)	ENSP00000401860.2:n.-122_-121del
ENST00000686757.1:c.-122_-121del (SLC22A5)	ENSP00000510721.1:n.-122_-121del
ENST00000687740.1:n.13_14del (SLC22A5)
ENST00000689271.1:c.-122_-121del (SLC22A5)	ENSP00000510797.1:n.-122_-121del
ENST00000690900.1:c.-122_-121del (SLC22A5)	ENSP00000510703.1:n.-122_-121del
ENST00000692413.1:c.-122_-121del (SLC22A5)	ENSP00000509374.1:n.-122_-121del
ENST00000693308.1:c.-122_-121del (SLC22A5)	ENSP00000509770.1:n.-122_-121del
ENST00000693763.1:n.13_14del (SLC22A5)
ENST00000245407.8:c.-122_-121del (SLC22A5) MANE Select	ENSP00000245407.3:n.-122_-121del
ENST00000245407.7:c.-122_-121del (SLC22A5)	ENSP00000245407.3:n.-122_-121del
NM_001308122.1:c.-122_-121del (SLC22A5)	NP_001295051.1:n.-122_-121del
NM_003060.3:c.-122_-121del (SLC22A5)	NP_003051.1:n.-122_-121del
NR_110997.1:n.65_66del (MIR3936HG)
XR_427718.1:n.148_149del (SLC22A5)
XR_948290.1:n.148_149del (SLC22A5)
XR_948291.1:n.148_149del (SLC22A5)
XR_001742215.1:n.148_149del (SLC22A5)
XR_001742216.1:n.148_149del (SLC22A5)
XR_427718.2:n.148_149del (SLC22A5)
XR_948290.2:n.148_149del (SLC22A5)
XR_948291.2:n.148_149del (SLC22A5)
NM_003060.4:c.-122_-121del (SLC22A5) MANE Select	NP_003051.1:n.-122_-121del
NM_001308122.2:c.-122_-121del (SLC22A5)	NP_001295051.1:n.-122_-121del