Canonical Allele Identifier: CA1583125032

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340633_132340634delinsCT , CM000667.2:g.132340633_132340634delinsCT	GRCh38
NC_000005.9:g.131676326_131676327delinsCT , CM000667.1:g.131676326_131676327delinsCT	GRCh37
NC_000005.8:g.131704225_131704226delinsCT	NCBI36
NG_012129.1:g.51182_51183delinsCT
NG_012129.2:g.51182_51183delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1513_1514delinsCT (SLC22A4) MANE Select	ENSP00000200652.3:p.Leu505=
ENST00000200652.3:c.1513_1514delinsCT (SLC22A4)	ENSP00000200652.3:p.Leu505=
NM_003059.2:c.1513_1514delinsCT (SLC22A4)	NP_003050.2:p.Leu505=
NR_110997.1:n.561-5708_561-5707delinsAG (MIR3936HG)
XM_006714675.2:c.985_986delinsCT (SLC22A4)	XP_006714738.1:p.Leu329=
XM_011543589.1:c.1237_1238delinsCT (SLC22A4)	XP_011541891.1:p.Leu413=
XM_006714675.4:c.985_986delinsCT (SLC22A4)	XP_006714738.1:p.Leu329=
XM_011543589.2:c.1237_1238delinsCT (SLC22A4)	XP_011541891.1:p.Leu413=
XM_017009776.1:c.985_986delinsCT (SLC22A4)	XP_016865265.1:p.Leu329=
NM_003059.3:c.1513_1514delinsCT (SLC22A4) MANE Select	NP_003050.2:p.Leu505=