Canonical Allele Identifier: CA360804163
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.131649455A>C (hg19) chr5:g.132313762A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313762A>C , CM000667.2:g.132313762A>C GRCh38
NC_000005.9:g.131649455A>C , CM000667.1:g.131649455A>C GRCh37
NC_000005.8:g.131677354A>C NCBI36
NG_012129.1:g.24311A>C
NG_012129.2:g.24311A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.646A>C (SLC22A4) MANE Select ENSP00000200652.3:p.Ile216Leu
ENST00000200652.3:c.646A>C (SLC22A4) ENSP00000200652.3:p.Ile216Leu
ENST00000491257.1:n.450A>C (SLC22A4)
NM_003059.2:c.646A>C (SLC22A4) NP_003050.2:p.Ile216Leu
NR_110997.1:n.825-1509T>G (MIR3936HG)
XM_006714675.2:c.118A>C (SLC22A4) XP_006714738.1:p.Ile40Leu
XM_011543589.1:c.542A>C (SLC22A4) XP_011541891.1:p.His181Pro
XM_006714675.4:c.118A>C (SLC22A4) XP_006714738.1:p.Ile40Leu
XM_011543589.2:c.542A>C (SLC22A4) XP_011541891.1:p.His181Pro
XM_017009776.1:c.118A>C (SLC22A4) XP_016865265.1:p.Ile40Leu
NM_003059.3:c.646A>C (SLC22A4) MANE Select NP_003050.2:p.Ile216Leu
Search 100 bp 5'
Search 100 bp 3'