Canonical Allele Identifier: CA1583124959
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

dbSNP Id: rs1751179338

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340476_132340479dup , CM000667.2:g.132340476_132340479dup GRCh38
NC_000005.9:g.131676169_131676172dup , CM000667.1:g.131676169_131676172dup GRCh37
NC_000005.8:g.131704068_131704071dup NCBI36
NG_012129.1:g.51025_51028dup
NG_012129.2:g.51025_51028dup

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1445-89_1445-86dup (SLC22A4) MANE Select ENSP00000200652.3:n.1445-89_1445-86dup
ENST00000200652.3:c.1445-89_1445-86dup (SLC22A4) ENSP00000200652.3:n.1445-89_1445-86dup
NM_003059.2:c.1445-89_1445-86dup (SLC22A4) NP_003050.2:n.1445-89_1445-86dup
NR_110997.1:n.561-5553_561-5550dup (MIR3936HG)
XM_006714675.2:c.917-89_917-86dup (SLC22A4) XP_006714738.1:n.917-89_917-86dup
XM_011543589.1:c.1169-89_1169-86dup (SLC22A4) XP_011541891.1:n.1169-89_1169-86dup
XM_006714675.4:c.917-89_917-86dup (SLC22A4) XP_006714738.1:n.917-89_917-86dup
XM_011543589.2:c.1169-89_1169-86dup (SLC22A4) XP_011541891.1:n.1169-89_1169-86dup
XM_017009776.1:c.917-89_917-86dup (SLC22A4) XP_016865265.1:n.917-89_917-86dup
NM_003059.3:c.1445-89_1445-86dup (SLC22A4) MANE Select NP_003050.2:n.1445-89_1445-86dup