Canonical Allele Identifier: CA2675194763

Gene: SLC22A5 MIR3936HG

Linked Data

• gnomAD v4: 5-132369711-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369711C>A , CM000667.2:g.132369711C>A	GRCh38
NC_000005.9:g.131705403C>A , CM000667.1:g.131705403C>A	GRCh37
NC_000005.8:g.131733302C>A	NCBI36
NG_008982.1:g.5003C>A
NG_008982.2:g.5008C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-262C>A (SLC22A5) MANE Select	ENSP00000245407.3:n.-262C>A
NM_001308122.1:c.-262C>A (SLC22A5)	NP_001295051.1:n.-262C>A
NM_003060.3:c.-262C>A (SLC22A5)	NP_003051.1:n.-262C>A
NR_110997.1:n.73+133G>T (MIR3936HG)
XR_427718.1:n.8C>A (SLC22A5)
XR_948290.1:n.8C>A (SLC22A5)
XR_948291.1:n.8C>A (SLC22A5)
XR_001742215.1:n.8C>A (SLC22A5)
XR_001742216.1:n.8C>A (SLC22A5)
XR_427718.2:n.8C>A (SLC22A5)
XR_948290.2:n.8C>A (SLC22A5)
XR_948291.2:n.8C>A (SLC22A5)
NM_003060.4:c.-262C>A (SLC22A5) MANE Select	NP_003051.1:n.-262C>A
NM_001308122.2:c.-262C>A (SLC22A5)	NP_001295051.1:n.-262C>A