Canonical Allele Identifier: CA1583118466
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313738A= , CM000667.2:g.132313738A= GRCh38
NC_000005.9:g.131649431A= , CM000667.1:g.131649431A= GRCh37
NC_000005.8:g.131677330A= NCBI36
NG_012129.1:g.24287A=
NG_012129.2:g.24287A=

Transcript Alleles

HGVS Amino-acid change
ENST00000200652.4:c.622A= (SLC22A4) MANE Select ENSP00000200652.3:p.Ile208=
ENST00000200652.3:c.622A= (SLC22A4) ENSP00000200652.3:p.Ile208=
ENST00000491257.1:n.426A= (SLC22A4)
NM_003059.2:c.622A= (SLC22A4) NP_003050.2:p.Ile208=
NR_110997.1:n.825-1485T= (MIR3936HG)
XM_006714675.2:c.94A= (SLC22A4) XP_006714738.1:p.Ile32=
XM_011543589.1:c.518A= (SLC22A4) XP_011541891.1:p.Asp173=
XM_006714675.4:c.94A= (SLC22A4) XP_006714738.1:p.Ile32=
XM_011543589.2:c.518A= (SLC22A4) XP_011541891.1:p.Asp173=
XM_017009776.1:c.94A= (SLC22A4) XP_016865265.1:p.Ile32=
NM_003059.3:c.622A= (SLC22A4) MANE Select NP_003050.2:p.Ile208=