Canonical Allele Identifier: CA360812870

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132340585-C-T
• MyVariant Identifiers: chr5:g.131676278C>T (hg19) ; chr5:g.132340585C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340585C>T , CM000667.2:g.132340585C>T	GRCh38
NC_000005.9:g.131676278C>T , CM000667.1:g.131676278C>T	GRCh37
NC_000005.8:g.131704177C>T	NCBI36
NG_012129.1:g.51134C>T
NG_012129.2:g.51134C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1465C>T (SLC22A4) MANE Select	ENSP00000200652.3:p.Pro489Ser
ENST00000200652.3:c.1465C>T (SLC22A4)	ENSP00000200652.3:p.Pro489Ser
NM_003059.2:c.1465C>T (SLC22A4)	NP_003050.2:p.Pro489Ser
NR_110997.1:n.561-5659G>A (MIR3936HG)
XM_006714675.2:c.937C>T (SLC22A4)	XP_006714738.1:p.Pro313Ser
XM_011543589.1:c.1189C>T (SLC22A4)	XP_011541891.1:p.Pro397Ser
XM_006714675.4:c.937C>T (SLC22A4)	XP_006714738.1:p.Pro313Ser
XM_011543589.2:c.1189C>T (SLC22A4)	XP_011541891.1:p.Pro397Ser
XM_017009776.1:c.937C>T (SLC22A4)	XP_016865265.1:p.Pro313Ser
NM_003059.3:c.1465C>T (SLC22A4) MANE Select	NP_003050.2:p.Pro489Ser