Canonical Allele Identifier: CA2768435834

Gene: SLC22A5 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369802C>G , CM000667.2:g.132369802C>G	GRCh38
NC_000005.9:g.131705494C>G , CM000667.1:g.131705494C>G	GRCh37
NC_000005.8:g.131733393C>G	NCBI36
NG_008982.1:g.5094C>G
NG_008982.2:g.5099C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000245407.8:c.-171C>G (SLC22A5) MANE Select	ENSP00000245407.3:n.-171C>G
ENST00000245407.7:c.-171C>G (SLC22A5)	ENSP00000245407.3:n.-171C>G
NM_001308122.1:c.-171C>G (SLC22A5)	NP_001295051.1:n.-171C>G
NM_003060.3:c.-171C>G (SLC22A5)	NP_003051.1:n.-171C>G
NR_110997.1:n.73+42G>C (MIR3936HG)
XR_427718.1:n.99C>G (SLC22A5)
XR_948290.1:n.99C>G (SLC22A5)
XR_948291.1:n.99C>G (SLC22A5)
XR_001742215.1:n.99C>G (SLC22A5)
XR_001742216.1:n.99C>G (SLC22A5)
XR_427718.2:n.99C>G (SLC22A5)
XR_948290.2:n.99C>G (SLC22A5)
XR_948291.2:n.99C>G (SLC22A5)
NM_003060.4:c.-171C>G (SLC22A5) MANE Select	NP_003051.1:n.-171C>G
NM_001308122.2:c.-171C>G (SLC22A5)	NP_001295051.1:n.-171C>G