Canonical Allele Identifier: CA446328800

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132313725-G-A
• MyVariant Identifiers: chr5:g.131649418G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313725G>A , CM000667.2:g.132313725G>A	GRCh38
NC_000005.9:g.131649418G>A , CM000667.1:g.131649418G>A	GRCh37
NC_000005.8:g.131677317G>A	NCBI36
NG_012129.1:g.24274G>A
NG_012129.2:g.24274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.609G>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Val203=
ENST00000200652.3:c.609G>A (SLC22A4)	ENSP00000200652.3:p.Val203=
ENST00000491257.1:n.413G>A (SLC22A4)
NM_003059.2:c.609G>A (SLC22A4)	NP_003050.2:p.Val203=
NR_110997.1:n.825-1472C>T (MIR3936HG)
XM_006714675.2:c.81G>A (SLC22A4)	XP_006714738.1:p.Val27=
XM_011543589.1:c.505G>A (SLC22A4)	XP_011541891.1:p.Gly169Arg
XM_006714675.4:c.81G>A (SLC22A4)	XP_006714738.1:p.Val27=
XM_011543589.2:c.505G>A (SLC22A4)	XP_011541891.1:p.Gly169Arg
XM_017009776.1:c.81G>A (SLC22A4)	XP_016865265.1:p.Val27=
NM_003059.3:c.609G>A (SLC22A4) MANE Select	NP_003050.2:p.Val203=