Canonical Allele Identifier: CA2675194999

Gene: SLC22A5 MIR3936HG

Linked Data

• gnomAD v4: 5-132369776-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369776T>A , CM000667.2:g.132369776T>A	GRCh38
NC_000005.9:g.131705468T>A , CM000667.1:g.131705468T>A	GRCh37
NC_000005.8:g.131733367T>A	NCBI36
NG_008982.1:g.5068T>A
NG_008982.2:g.5073T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000245407.8:c.-197T>A (SLC22A5) MANE Select	ENSP00000245407.3:n.-197T>A
ENST00000245407.7:c.-197T>A (SLC22A5)	ENSP00000245407.3:n.-197T>A
NM_001308122.1:c.-197T>A (SLC22A5)	NP_001295051.1:n.-197T>A
NM_003060.3:c.-197T>A (SLC22A5)	NP_003051.1:n.-197T>A
NR_110997.1:n.73+68A>T (MIR3936HG)
XR_427718.1:n.73T>A (SLC22A5)
XR_948290.1:n.73T>A (SLC22A5)
XR_948291.1:n.73T>A (SLC22A5)
XR_001742215.1:n.73T>A (SLC22A5)
XR_001742216.1:n.73T>A (SLC22A5)
XR_427718.2:n.73T>A (SLC22A5)
XR_948290.2:n.73T>A (SLC22A5)
XR_948291.2:n.73T>A (SLC22A5)
NM_003060.4:c.-197T>A (SLC22A5) MANE Select	NP_003051.1:n.-197T>A
NM_001308122.2:c.-197T>A (SLC22A5)	NP_001295051.1:n.-197T>A