Canonical Allele Identifier: CA1583124893
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340358A= , CM000667.2:g.132340358A= GRCh38
NC_000005.9:g.131676051A= , CM000667.1:g.131676051A= GRCh37
NC_000005.8:g.131703950A= NCBI36
NG_012129.1:g.50907A=
NG_012129.2:g.50907A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1445-207A= (SLC22A4) MANE Select ENSP00000200652.3:n.1445-207A=
ENST00000200652.3:c.1445-207A= (SLC22A4) ENSP00000200652.3:n.1445-207A=
NM_003059.2:c.1445-207A= (SLC22A4) NP_003050.2:n.1445-207A=
NR_110997.1:n.561-5432T= (MIR3936HG)
XM_006714675.2:c.917-207A= (SLC22A4) XP_006714738.1:n.917-207A=
XM_011543589.1:c.1169-207A= (SLC22A4) XP_011541891.1:n.1169-207A=
XM_006714675.4:c.917-207A= (SLC22A4) XP_006714738.1:n.917-207A=
XM_011543589.2:c.1169-207A= (SLC22A4) XP_011541891.1:n.1169-207A=
XM_017009776.1:c.917-207A= (SLC22A4) XP_016865265.1:n.917-207A=
NM_003059.3:c.1445-207A= (SLC22A4) MANE Select NP_003050.2:n.1445-207A=