Canonical Allele Identifier: CA2675195071

Gene: SLC22A5 MIR3936HG

Linked Data

• gnomAD v4: 5-132369801-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369801G>T , CM000667.2:g.132369801G>T	GRCh38
NC_000005.9:g.131705493G>T , CM000667.1:g.131705493G>T	GRCh37
NC_000005.8:g.131733392G>T	NCBI36
NG_008982.1:g.5093G>T
NG_008982.2:g.5098G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-172G>T (SLC22A5) MANE Select	ENSP00000245407.3:n.-172G>T
ENST00000245407.7:c.-172G>T (SLC22A5)	ENSP00000245407.3:n.-172G>T
NM_001308122.1:c.-172G>T (SLC22A5)	NP_001295051.1:n.-172G>T
NM_003060.3:c.-172G>T (SLC22A5)	NP_003051.1:n.-172G>T
NR_110997.1:n.73+43C>A (MIR3936HG)
XR_427718.1:n.98G>T (SLC22A5)
XR_948290.1:n.98G>T (SLC22A5)
XR_948291.1:n.98G>T (SLC22A5)
XR_001742215.1:n.98G>T (SLC22A5)
XR_001742216.1:n.98G>T (SLC22A5)
XR_427718.2:n.98G>T (SLC22A5)
XR_948290.2:n.98G>T (SLC22A5)
XR_948291.2:n.98G>T (SLC22A5)
NM_003060.4:c.-172G>T (SLC22A5) MANE Select	NP_003051.1:n.-172G>T
NM_001308122.2:c.-172G>T (SLC22A5)	NP_001295051.1:n.-172G>T