Canonical Allele Identifier: CA1583118304

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313612_132313613delinsAG , CM000667.2:g.132313612_132313613delinsAG	GRCh38
NC_000005.9:g.131649305_131649306delinsAG , CM000667.1:g.131649305_131649306delinsAG	GRCh37
NC_000005.8:g.131677204_131677205delinsAG	NCBI36
NG_012129.1:g.24161_24162delinsAG
NG_012129.2:g.24161_24162delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-2_498-1delinsAG (SLC22A4) MANE Select	ENSP00000200652.3:n.498-2_498-1delinsAG
ENST00000200652.3:c.498-2_498-1delinsAG (SLC22A4)	ENSP00000200652.3:n.498-2_498-1delinsAG
ENST00000491257.1:n.302-2_302-1delinsAG (SLC22A4)
NM_003059.2:c.498-2_498-1delinsAG (SLC22A4)	NP_003050.2:n.498-2_498-1delinsAG
NR_110997.1:n.825-1360_825-1359delinsCT (MIR3936HG)
XM_006714675.2:c.-31-2_-31-1delinsAG (SLC22A4)	XP_006714738.1:n.-31-2_-31-1delinsAG
XM_011543589.1:c.394-2_394-1delinsAG (SLC22A4)	XP_011541891.1:n.394-2_394-1delinsAG
XM_006714675.4:c.-31-2_-31-1delinsAG (SLC22A4)	XP_006714738.1:n.-31-2_-31-1delinsAG
XM_011543589.2:c.394-2_394-1delinsAG (SLC22A4)	XP_011541891.1:n.394-2_394-1delinsAG
XM_017009776.1:c.-31-2_-31-1delinsAG (SLC22A4)	XP_016865265.1:n.-31-2_-31-1delinsAG
NM_003059.3:c.498-2_498-1delinsAG (SLC22A4) MANE Select	NP_003050.2:n.498-2_498-1delinsAG