Canonical Allele Identifier: CA1583124913

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1751175170

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340390_132340391insATGT , CM000667.2:g.132340390_132340391insATGT	GRCh38
NC_000005.9:g.131676083_131676084insATGT , CM000667.1:g.131676083_131676084insATGT	GRCh37
NC_000005.8:g.131703982_131703983insATGT	NCBI36
NG_012129.1:g.50939_50940insATGT
NG_012129.2:g.50939_50940insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1445-175_1445-174insATGT (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-175_1445-174insATGT
ENST00000200652.3:c.1445-175_1445-174insATGT (SLC22A4)	ENSP00000200652.3:n.1445-175_1445-174insATGT
NM_003059.2:c.1445-175_1445-174insATGT (SLC22A4)	NP_003050.2:n.1445-175_1445-174insATGT
NR_110997.1:n.561-5464_561-5463insCATA (MIR3936HG)
XM_006714675.2:c.917-175_917-174insATGT (SLC22A4)	XP_006714738.1:n.917-175_917-174insATGT
XM_011543589.1:c.1169-175_1169-174insATGT (SLC22A4)	XP_011541891.1:n.1169-175_1169-174insATGT
XM_006714675.4:c.917-175_917-174insATGT (SLC22A4)	XP_006714738.1:n.917-175_917-174insATGT
XM_011543589.2:c.1169-175_1169-174insATGT (SLC22A4)	XP_011541891.1:n.1169-175_1169-174insATGT
XM_017009776.1:c.917-175_917-174insATGT (SLC22A4)	XP_016865265.1:n.917-175_917-174insATGT
NM_003059.3:c.1445-175_1445-174insATGT (SLC22A4) MANE Select	NP_003050.2:n.1445-175_1445-174insATGT