Canonical Allele Identifier: CA2768422477

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340641_132340649del , CM000667.2:g.132340641_132340649del	GRCh38
NC_000005.9:g.131676334_131676342del , CM000667.1:g.131676334_131676342del	GRCh37
NC_000005.8:g.131704233_131704241del	NCBI36
NG_012129.1:g.51190_51198del
NG_012129.2:g.51190_51198del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1521_1529del (SLC22A4) MANE Select	ENSP00000200652.3:p.Pro508_Ser510del
ENST00000200652.3:c.1521_1529del (SLC22A4)	ENSP00000200652.3:p.Pro508_Ser510del
NM_003059.2:c.1521_1529del (SLC22A4)	NP_003050.2:p.Pro508_Ser510del
NR_110997.1:n.561-5723_561-5715del (MIR3936HG)
XM_006714675.2:c.993_1001del (SLC22A4)	XP_006714738.1:p.Pro332_Ser334del
XM_011543589.1:c.1245_1253del (SLC22A4)	XP_011541891.1:p.Pro416_Ser418del
XM_006714675.4:c.993_1001del (SLC22A4)	XP_006714738.1:p.Pro332_Ser334del
XM_011543589.2:c.1245_1253del (SLC22A4)	XP_011541891.1:p.Pro416_Ser418del
XM_017009776.1:c.993_1001del (SLC22A4)	XP_016865265.1:p.Pro332_Ser334del
NM_003059.3:c.1521_1529del (SLC22A4) MANE Select	NP_003050.2:p.Pro508_Ser510del