Canonical Allele Identifier: CA2675193390

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132340643-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340644del , CM000667.2:g.132340644del	GRCh38
NC_000005.9:g.131676337del , CM000667.1:g.131676337del	GRCh37
NC_000005.8:g.131704236del	NCBI36
NG_012129.1:g.51193del
NG_012129.2:g.51193del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1524del (SLC22A4) MANE Select	ENSP00000200652.3:p.Glu509LysfsTer5
ENST00000200652.3:c.1524del (SLC22A4)	ENSP00000200652.3:p.Glu509LysfsTer5
NM_003059.2:c.1524del (SLC22A4)	NP_003050.2:p.Glu509LysfsTer5
NR_110997.1:n.561-5718del (MIR3936HG)
XM_006714675.2:c.996del (SLC22A4)	XP_006714738.1:p.Glu333LysfsTer5
XM_011543589.1:c.1248del (SLC22A4)	XP_011541891.1:p.Glu417LysfsTer5
XM_006714675.4:c.996del (SLC22A4)	XP_006714738.1:p.Glu333LysfsTer5
XM_011543589.2:c.1248del (SLC22A4)	XP_011541891.1:p.Glu417LysfsTer5
XM_017009776.1:c.996del (SLC22A4)	XP_016865265.1:p.Glu333LysfsTer5
NM_003059.3:c.1524del (SLC22A4) MANE Select	NP_003050.2:p.Glu509LysfsTer5