Canonical Allele Identifier: CA360813054

Gene: SLC22A4 MIR3936HG

Linked Data

• MyVariant Identifiers: chr5:g.131676308C>A (hg19) ; chr5:g.132340615C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340615C>A , CM000667.2:g.132340615C>A	GRCh38
NC_000005.9:g.131676308C>A , CM000667.1:g.131676308C>A	GRCh37
NC_000005.8:g.131704207C>A	NCBI36
NG_012129.1:g.51164C>A
NG_012129.2:g.51164C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1495C>A (SLC22A4) MANE Select	ENSP00000200652.3:p.Leu499Met
ENST00000200652.3:c.1495C>A (SLC22A4)	ENSP00000200652.3:p.Leu499Met
NM_003059.2:c.1495C>A (SLC22A4)	NP_003050.2:p.Leu499Met
NR_110997.1:n.561-5689G>T (MIR3936HG)
XM_006714675.2:c.967C>A (SLC22A4)	XP_006714738.1:p.Leu323Met
XM_011543589.1:c.1219C>A (SLC22A4)	XP_011541891.1:p.Leu407Met
XM_006714675.4:c.967C>A (SLC22A4)	XP_006714738.1:p.Leu323Met
XM_011543589.2:c.1219C>A (SLC22A4)	XP_011541891.1:p.Leu407Met
XM_017009776.1:c.967C>A (SLC22A4)	XP_016865265.1:p.Leu323Met
NM_003059.3:c.1495C>A (SLC22A4) MANE Select	NP_003050.2:p.Leu499Met