Canonical Allele Identifier: CA1583124880
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132340308_132340310delinsCAT , CM000667.2:g.132340308_132340310delinsCAT GRCh38
NC_000005.9:g.131676001_131676003delinsCAT , CM000667.1:g.131676001_131676003delinsCAT GRCh37
NC_000005.8:g.131703900_131703902delinsCAT NCBI36
NG_012129.1:g.50857_50859delinsCAT
NG_012129.2:g.50857_50859delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.1445-257_1445-255delinsCAT (SLC22A4) MANE Select ENSP00000200652.3:n.1445-257_1445-255delinsCAT
ENST00000200652.3:c.1445-257_1445-255delinsCAT (SLC22A4) ENSP00000200652.3:n.1445-257_1445-255delinsCAT
NM_003059.2:c.1445-257_1445-255delinsCAT (SLC22A4) NP_003050.2:n.1445-257_1445-255delinsCAT
NR_110997.1:n.561-5384_561-5382delinsATG (MIR3936HG)
XM_006714675.2:c.917-257_917-255delinsCAT (SLC22A4) XP_006714738.1:n.917-257_917-255delinsCAT
XM_011543589.1:c.1169-257_1169-255delinsCAT (SLC22A4) XP_011541891.1:n.1169-257_1169-255delinsCAT
XM_006714675.4:c.917-257_917-255delinsCAT (SLC22A4) XP_006714738.1:n.917-257_917-255delinsCAT
XM_011543589.2:c.1169-257_1169-255delinsCAT (SLC22A4) XP_011541891.1:n.1169-257_1169-255delinsCAT
XM_017009776.1:c.917-257_917-255delinsCAT (SLC22A4) XP_016865265.1:n.917-257_917-255delinsCAT
NM_003059.3:c.1445-257_1445-255delinsCAT (SLC22A4) MANE Select NP_003050.2:n.1445-257_1445-255delinsCAT