Canonical Allele Identifier: CA913108214

Gene: SLC22A5 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131705534_131705562del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369842_132369870del , CM000667.2:g.132369842_132369870del	GRCh38
NC_000005.9:g.131705534_131705562del , CM000667.1:g.131705534_131705562del	GRCh37
NC_000005.8:g.131733433_131733461del	NCBI36
NG_008982.1:g.5134_5162del
NG_008982.2:g.5139_5167del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000415928.6:c.-131_-103del (SLC22A5)	ENSP00000388838.2:n.-131_-103del
ENST00000435065.7:c.-131_-103del (SLC22A5)	ENSP00000402760.2:n.-131_-103del
ENST00000448810.6:c.-131_-103del (SLC22A5)	ENSP00000401860.2:n.-131_-103del
ENST00000686757.1:c.-131_-103del (SLC22A5)	ENSP00000510721.1:n.-131_-103del
ENST00000687740.1:n.4_32del (SLC22A5)
ENST00000689271.1:c.-131_-103del (SLC22A5)	ENSP00000510797.1:n.-131_-103del
ENST00000690900.1:c.-131_-103del (SLC22A5)	ENSP00000510703.1:n.-131_-103del
ENST00000692413.1:c.-131_-103del (SLC22A5)	ENSP00000509374.1:n.-131_-103del
ENST00000693308.1:c.-131_-103del (SLC22A5)	ENSP00000509770.1:n.-131_-103del
ENST00000693763.1:n.4_32del (SLC22A5)
ENST00000245407.8:c.-131_-103del (SLC22A5) MANE Select	ENSP00000245407.3:n.-131_-103del
ENST00000245407.7:c.-131_-103del (SLC22A5)	ENSP00000245407.3:n.-131_-103del
NM_001308122.1:c.-131_-103del (SLC22A5)	NP_001295051.1:n.-131_-103del
NM_003060.3:c.-131_-103del (SLC22A5)	NP_003051.1:n.-131_-103del
NR_110997.1:n.47_73+2del (MIR3936HG)
XR_427718.1:n.139_167del (SLC22A5)
XR_948290.1:n.139_167del (SLC22A5)
XR_948291.1:n.139_167del (SLC22A5)
XR_001742215.1:n.139_167del (SLC22A5)
XR_001742216.1:n.139_167del (SLC22A5)
XR_427718.2:n.139_167del (SLC22A5)
XR_948290.2:n.139_167del (SLC22A5)
XR_948291.2:n.139_167del (SLC22A5)
NM_003060.4:c.-131_-103del (SLC22A5) MANE Select	NP_003051.1:n.-131_-103del
NM_001308122.2:c.-131_-103del (SLC22A5)	NP_001295051.1:n.-131_-103del