Canonical Allele Identifier: CA1583118284

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313588_132313589delinsGT , CM000667.2:g.132313588_132313589delinsGT	GRCh38
NC_000005.9:g.131649281_131649282delinsGT , CM000667.1:g.131649281_131649282delinsGT	GRCh37
NC_000005.8:g.131677180_131677181delinsGT	NCBI36
NG_012129.1:g.24137_24138delinsGT
NG_012129.2:g.24137_24138delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-26_498-25delinsGT (SLC22A4) MANE Select	ENSP00000200652.3:n.498-26_498-25delinsGT
ENST00000200652.3:c.498-26_498-25delinsGT (SLC22A4)	ENSP00000200652.3:n.498-26_498-25delinsGT
ENST00000491257.1:n.302-26_302-25delinsGT (SLC22A4)
NM_003059.2:c.498-26_498-25delinsGT (SLC22A4)	NP_003050.2:n.498-26_498-25delinsGT
NR_110997.1:n.825-1336_825-1335delinsAC (MIR3936HG)
XM_006714675.2:c.-31-26_-31-25delinsGT (SLC22A4)	XP_006714738.1:n.-31-26_-31-25delinsGT
XM_011543589.1:c.394-26_394-25delinsGT (SLC22A4)	XP_011541891.1:n.394-26_394-25delinsGT
XM_006714675.4:c.-31-26_-31-25delinsGT (SLC22A4)	XP_006714738.1:n.-31-26_-31-25delinsGT
XM_011543589.2:c.394-26_394-25delinsGT (SLC22A4)	XP_011541891.1:n.394-26_394-25delinsGT
XM_017009776.1:c.-31-26_-31-25delinsGT (SLC22A4)	XP_016865265.1:n.-31-26_-31-25delinsGT
NM_003059.3:c.498-26_498-25delinsGT (SLC22A4) MANE Select	NP_003050.2:n.498-26_498-25delinsGT