Canonical Allele Identifier: CA1583118434

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313710_132313714delinsGTTAT , CM000667.2:g.132313710_132313714delinsGTTAT	GRCh38
NC_000005.9:g.131649403_131649407delinsGTTAT , CM000667.1:g.131649403_131649407delinsGTTAT	GRCh37
NC_000005.8:g.131677302_131677306delinsGTTAT	NCBI36
NG_012129.1:g.24259_24263delinsGTTAT
NG_012129.2:g.24259_24263delinsGTTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.594_598delinsGTTAT (SLC22A4) MANE Select	ENSP00000200652.3:p.Val198=
ENST00000200652.3:c.594_598delinsGTTAT (SLC22A4)	ENSP00000200652.3:p.Val198=
ENST00000491257.1:n.398_402delinsGTTAT (SLC22A4)
NM_003059.2:c.594_598delinsGTTAT (SLC22A4)	NP_003050.2:p.Val198=
NR_110997.1:n.825-1461_825-1457delinsATAAC (MIR3936HG)
XM_006714675.2:c.66_70delinsGTTAT (SLC22A4)	XP_006714738.1:p.Val22=
XM_011543589.1:c.490_494delinsGTTAT (SLC22A4)	XP_011541891.1:p.Val164=
XM_006714675.4:c.66_70delinsGTTAT (SLC22A4)	XP_006714738.1:p.Val22=
XM_011543589.2:c.490_494delinsGTTAT (SLC22A4)	XP_011541891.1:p.Val164=
XM_017009776.1:c.66_70delinsGTTAT (SLC22A4)	XP_016865265.1:p.Val22=
NM_003059.3:c.594_598delinsGTTAT (SLC22A4) MANE Select	NP_003050.2:p.Val198=