Canonical Allele Identifier: CA2521429557

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132313567_132313569del , CM000667.2:g.132313567_132313569del	GRCh38
NC_000005.9:g.131649260_131649262del , CM000667.1:g.131649260_131649262del	GRCh37
NC_000005.8:g.131677159_131677161del	NCBI36
NG_012129.1:g.24116_24118del
NG_012129.2:g.24116_24118del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.498-47_498-45del (SLC22A4) MANE Select	ENSP00000200652.3:n.498-47_498-45del
ENST00000200652.3:c.498-47_498-45del (SLC22A4)	ENSP00000200652.3:n.498-47_498-45del
ENST00000491257.1:n.302-47_302-45del (SLC22A4)
NM_003059.2:c.498-47_498-45del (SLC22A4)	NP_003050.2:n.498-47_498-45del
NR_110997.1:n.825-1316_825-1314del (MIR3936HG)
XM_006714675.2:c.-31-47_-31-45del (SLC22A4)	XP_006714738.1:n.-31-47_-31-45del
XM_011543589.1:c.394-47_394-45del (SLC22A4)	XP_011541891.1:n.394-47_394-45del
XM_006714675.4:c.-31-47_-31-45del (SLC22A4)	XP_006714738.1:n.-31-47_-31-45del
XM_011543589.2:c.394-47_394-45del (SLC22A4)	XP_011541891.1:n.394-47_394-45del
XM_017009776.1:c.-31-47_-31-45del (SLC22A4)	XP_016865265.1:n.-31-47_-31-45del
NM_003059.3:c.498-47_498-45del (SLC22A4) MANE Select	NP_003050.2:n.498-47_498-45del