Canonical Allele Identifier: CA1583125022

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340610C= , CM000667.2:g.132340610C=	GRCh38
NC_000005.9:g.131676303C= , CM000667.1:g.131676303C=	GRCh37
NC_000005.8:g.131704202C=	NCBI36
NG_012129.1:g.51159C=
NG_012129.2:g.51159C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1490C= (SLC22A4) MANE Select	ENSP00000200652.3:p.Thr497=
ENST00000200652.3:c.1490C= (SLC22A4)	ENSP00000200652.3:p.Thr497=
NM_003059.2:c.1490C= (SLC22A4)	NP_003050.2:p.Thr497=
NR_110997.1:n.561-5684G= (MIR3936HG)
XM_006714675.2:c.962C= (SLC22A4)	XP_006714738.1:p.Thr321=
XM_011543589.1:c.1214C= (SLC22A4)	XP_011541891.1:p.Thr405=
XM_006714675.4:c.962C= (SLC22A4)	XP_006714738.1:p.Thr321=
XM_011543589.2:c.1214C= (SLC22A4)	XP_011541891.1:p.Thr405=
XM_017009776.1:c.962C= (SLC22A4)	XP_016865265.1:p.Thr321=
NM_003059.3:c.1490C= (SLC22A4) MANE Select	NP_003050.2:p.Thr497=