Canonical Allele Identifier: CA2675195093

Gene: SLC22A5 MIR3936HG

Linked Data

• gnomAD v4: 5-132369809-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369809A>C , CM000667.2:g.132369809A>C	GRCh38
NC_000005.9:g.131705501A>C , CM000667.1:g.131705501A>C	GRCh37
NC_000005.8:g.131733400A>C	NCBI36
NG_008982.1:g.5101A>C
NG_008982.2:g.5106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-164A>C (SLC22A5) MANE Select	ENSP00000245407.3:n.-164A>C
ENST00000245407.7:c.-164A>C (SLC22A5)	ENSP00000245407.3:n.-164A>C
NM_001308122.1:c.-164A>C (SLC22A5)	NP_001295051.1:n.-164A>C
NM_003060.3:c.-164A>C (SLC22A5)	NP_003051.1:n.-164A>C
NR_110997.1:n.73+35T>G (MIR3936HG)
XR_427718.1:n.106A>C (SLC22A5)
XR_948290.1:n.106A>C (SLC22A5)
XR_948291.1:n.106A>C (SLC22A5)
XR_001742215.1:n.106A>C (SLC22A5)
XR_001742216.1:n.106A>C (SLC22A5)
XR_427718.2:n.106A>C (SLC22A5)
XR_948290.2:n.106A>C (SLC22A5)
XR_948291.2:n.106A>C (SLC22A5)
NM_003060.4:c.-164A>C (SLC22A5) MANE Select	NP_003051.1:n.-164A>C
NM_001308122.2:c.-164A>C (SLC22A5)	NP_001295051.1:n.-164A>C