Canonical Allele Identifier: CA1583137489

Gene: SLC22A5 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132369834G= , CM000667.2:g.132369834G=	GRCh38
NC_000005.9:g.131705526G= , CM000667.1:g.131705526G=	GRCh37
NC_000005.8:g.131733425G=	NCBI36
NG_008982.1:g.5126G=
NG_008982.2:g.5131G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435065.7:c.-139G= (SLC22A5)	ENSP00000402760.2:n.-139G=
ENST00000245407.8:c.-139G= (SLC22A5) MANE Select	ENSP00000245407.3:n.-139G=
ENST00000245407.7:c.-139G= (SLC22A5)	ENSP00000245407.3:n.-139G=
NM_001308122.1:c.-139G= (SLC22A5)	NP_001295051.1:n.-139G=
NM_003060.3:c.-139G= (SLC22A5)	NP_003051.1:n.-139G=
NR_110997.1:n.73+10C= (MIR3936HG)
XR_427718.1:n.131G= (SLC22A5)
XR_948290.1:n.131G= (SLC22A5)
XR_948291.1:n.131G= (SLC22A5)
XR_001742215.1:n.131G= (SLC22A5)
XR_001742216.1:n.131G= (SLC22A5)
XR_427718.2:n.131G= (SLC22A5)
XR_948290.2:n.131G= (SLC22A5)
XR_948291.2:n.131G= (SLC22A5)
NM_003060.4:c.-139G= (SLC22A5) MANE Select	NP_003051.1:n.-139G=
NM_001308122.2:c.-139G= (SLC22A5)	NP_001295051.1:n.-139G=