Canonical Allele Identifier: CA446330140

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132327296C>A , CM000667.2:g.132327296C>A	GRCh38
NC_000005.9:g.131662989C>A , CM000667.1:g.131662989C>A	GRCh37
NC_000005.8:g.131690888C>A	NCBI36
NG_012129.1:g.37845C>A
NG_012129.2:g.37845C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.844C>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Arg282=
ENST00000200652.3:c.844C>A (SLC22A4)	ENSP00000200652.3:p.Arg282=
ENST00000425923.1:n.374C>A (SLC22A4)
NM_003059.2:c.844C>A (SLC22A4)	NP_003050.2:p.Arg282=
NR_110997.1:n.824+4893G>T (MIR3936HG)
XM_006714675.2:c.316C>A (SLC22A4)	XP_006714738.1:p.Arg106=
XM_011543589.1:c.568C>A (SLC22A4)	XP_011541891.1:p.Arg190=
XM_006714675.4:c.316C>A (SLC22A4)	XP_006714738.1:p.Arg106=
XM_011543589.2:c.568C>A (SLC22A4)	XP_011541891.1:p.Arg190=
XM_017009776.1:c.316C>A (SLC22A4)	XP_016865265.1:p.Arg106=
NM_003059.3:c.844C>A (SLC22A4) MANE Select	NP_003050.2:p.Arg282=