Canonical Allele Identifier: CA1583124983
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340527C= , CM000667.2:g.132340527C= GRCh38
NC_000005.9:g.131676220C= , CM000667.1:g.131676220C= GRCh37
NC_000005.8:g.131704119C= NCBI36
NG_012129.1:g.51076C=
NG_012129.2:g.51076C=

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.1445-38C= (SLC22A4) MANE Select ENSP00000200652.3:n.1445-38C=
ENST00000200652.3:c.1445-38C= (SLC22A4) ENSP00000200652.3:n.1445-38C=
NM_003059.2:c.1445-38C= (SLC22A4) NP_003050.2:n.1445-38C=
NR_110997.1:n.561-5601G= (MIR3936HG)
XM_006714675.2:c.917-38C= (SLC22A4) XP_006714738.1:n.917-38C=
XM_011543589.1:c.1169-38C= (SLC22A4) XP_011541891.1:n.1169-38C=
XM_006714675.4:c.917-38C= (SLC22A4) XP_006714738.1:n.917-38C=
XM_011543589.2:c.1169-38C= (SLC22A4) XP_011541891.1:n.1169-38C=
XM_017009776.1:c.917-38C= (SLC22A4) XP_016865265.1:n.917-38C=
NM_003059.3:c.1445-38C= (SLC22A4) MANE Select NP_003050.2:n.1445-38C=