Canonical Allele Identifier: CA1583118425

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313702T= , CM000667.2:g.132313702T=	GRCh38
NC_000005.9:g.131649395T= , CM000667.1:g.131649395T=	GRCh37
NC_000005.8:g.131677294T=	NCBI36
NG_012129.1:g.24251T=
NG_012129.2:g.24251T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.586T= (SLC22A4) MANE Select	ENSP00000200652.3:p.Phe196=
ENST00000200652.3:c.586T= (SLC22A4)	ENSP00000200652.3:p.Phe196=
ENST00000491257.1:n.390T= (SLC22A4)
NM_003059.2:c.586T= (SLC22A4)	NP_003050.2:p.Phe196=
NR_110997.1:n.825-1449A= (MIR3936HG)
XM_006714675.2:c.58T= (SLC22A4)	XP_006714738.1:p.Phe20=
XM_011543589.1:c.482T= (SLC22A4)	XP_011541891.1:p.Val161=
XM_006714675.4:c.58T= (SLC22A4)	XP_006714738.1:p.Phe20=
XM_011543589.2:c.482T= (SLC22A4)	XP_011541891.1:p.Val161=
XM_017009776.1:c.58T= (SLC22A4)	XP_016865265.1:p.Phe20=
NM_003059.3:c.586T= (SLC22A4) MANE Select	NP_003050.2:p.Phe196=