Canonical Allele Identifier: CA360804041
Gene: SLC22A4 HGNC NCBI
MIR3936HG HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.131649411T>A (hg19) chr5:g.132313718T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132313718T>A , CM000667.2:g.132313718T>A GRCh38
NC_000005.9:g.131649411T>A , CM000667.1:g.131649411T>A GRCh37
NC_000005.8:g.131677310T>A NCBI36
NG_012129.1:g.24267T>A
NG_012129.2:g.24267T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000200652.4:c.602T>A (SLC22A4) MANE Select ENSP00000200652.3:p.Val201Asp
ENST00000200652.3:c.602T>A (SLC22A4) ENSP00000200652.3:p.Val201Asp
ENST00000491257.1:n.406T>A (SLC22A4)
NM_003059.2:c.602T>A (SLC22A4) NP_003050.2:p.Val201Asp
NR_110997.1:n.825-1465A>T (MIR3936HG)
XM_006714675.2:c.74T>A (SLC22A4) XP_006714738.1:p.Val25Asp
XM_011543589.1:c.498T>A (SLC22A4) XP_011541891.1:p.Cys166Ter
XM_006714675.4:c.74T>A (SLC22A4) XP_006714738.1:p.Val25Asp
XM_011543589.2:c.498T>A (SLC22A4) XP_011541891.1:p.Cys166Ter
XM_017009776.1:c.74T>A (SLC22A4) XP_016865265.1:p.Val25Asp
NM_003059.3:c.602T>A (SLC22A4) MANE Select NP_003050.2:p.Val201Asp
Search 100 bp 5'
Search 100 bp 3'