Canonical Allele Identifier: CA2740684044

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313805_132313806insGTGT , CM000667.2:g.132313805_132313806insGTGT	GRCh38
NC_000005.9:g.131649498_131649499insGTGT , CM000667.1:g.131649498_131649499insGTGT	GRCh37
NC_000005.8:g.131677397_131677398insGTGT	NCBI36
NG_012129.1:g.24354_24355insGTGT
NG_012129.2:g.24354_24355insGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.652+37_652+38insGTGT (SLC22A4) MANE Select	ENSP00000200652.3:n.652+37_652+38insGTGT
ENST00000200652.3:c.652+37_652+38insGTGT (SLC22A4)	ENSP00000200652.3:n.652+37_652+38insGTGT
ENST00000491257.1:n.456+37_456+38insGTGT (SLC22A4)
NM_003059.2:c.652+37_652+38insGTGT (SLC22A4)	NP_003050.2:n.652+37_652+38insGTGT
NR_110997.1:n.825-1552_825-1551insCACA (MIR3936HG)
XM_006714675.2:c.124+37_124+38insGTGT (SLC22A4)	XP_006714738.1:n.124+37_124+38insGTGT
XM_011543589.1:c.548+37_548+38insGTGT (SLC22A4)	XP_011541891.1:n.548+37_548+38insGTGT
XM_006714675.4:c.124+37_124+38insGTGT (SLC22A4)	XP_006714738.1:n.124+37_124+38insGTGT
XM_011543589.2:c.548+37_548+38insGTGT (SLC22A4)	XP_011541891.1:n.548+37_548+38insGTGT
XM_017009776.1:c.124+37_124+38insGTGT (SLC22A4)	XP_016865265.1:n.124+37_124+38insGTGT
NM_003059.3:c.652+37_652+38insGTGT (SLC22A4) MANE Select	NP_003050.2:n.652+37_652+38insGTGT