Canonical Allele Identifier: CA1583118322

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313630G= , CM000667.2:g.132313630G=	GRCh38
NC_000005.9:g.131649323G= , CM000667.1:g.131649323G=	GRCh37
NC_000005.8:g.131677222G=	NCBI36
NG_012129.1:g.24179G=
NG_012129.2:g.24179G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.514G= (SLC22A4) MANE Select	ENSP00000200652.3:p.Val172=
ENST00000200652.3:c.514G= (SLC22A4)	ENSP00000200652.3:p.Val172=
ENST00000491257.1:n.318G= (SLC22A4)
NM_003059.2:c.514G= (SLC22A4)	NP_003050.2:p.Val172=
NR_110997.1:n.825-1377C= (MIR3936HG)
XM_006714675.2:c.-15G= (SLC22A4)	XP_006714738.1:n.-15G=
XM_011543589.1:c.410G= (SLC22A4)	XP_011541891.1:p.Arg137=
XM_006714675.4:c.-15G= (SLC22A4)	XP_006714738.1:n.-15G=
XM_011543589.2:c.410G= (SLC22A4)	XP_011541891.1:p.Arg137=
XM_017009776.1:c.-15G= (SLC22A4)	XP_016865265.1:n.-15G=
NM_003059.3:c.514G= (SLC22A4) MANE Select	NP_003050.2:p.Val172=