Canonical Allele Identifier: CA360803885

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131649342C>T (hg19) ; chr5:g.132313649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313649C>T , CM000667.2:g.132313649C>T	GRCh38
NC_000005.9:g.131649342C>T , CM000667.1:g.131649342C>T	GRCh37
NC_000005.8:g.131677241C>T	NCBI36
NG_012129.1:g.24198C>T
NG_012129.2:g.24198C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.533C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Ala178Val
ENST00000200652.3:c.533C>T (SLC22A4)	ENSP00000200652.3:p.Ala178Val
ENST00000491257.1:n.337C>T (SLC22A4)
NM_003059.2:c.533C>T (SLC22A4)	NP_003050.2:p.Ala178Val
NR_110997.1:n.825-1396G>A (MIR3936HG)
XM_006714675.2:c.5C>T (SLC22A4)	XP_006714738.1:p.Ala2Val
XM_011543589.1:c.429C>T (SLC22A4)	XP_011541891.1:p.Gly143=
XM_006714675.4:c.5C>T (SLC22A4)	XP_006714738.1:p.Ala2Val
XM_011543589.2:c.429C>T (SLC22A4)	XP_011541891.1:p.Gly143=
XM_017009776.1:c.5C>T (SLC22A4)	XP_016865265.1:p.Ala2Val
NM_003059.3:c.533C>T (SLC22A4) MANE Select	NP_003050.2:p.Ala178Val