Canonical Allele Identifier: CA1583124992

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340541_132340542delinsGT , CM000667.2:g.132340541_132340542delinsGT	GRCh38
NC_000005.9:g.131676234_131676235delinsGT , CM000667.1:g.131676234_131676235delinsGT	GRCh37
NC_000005.8:g.131704133_131704134delinsGT	NCBI36
NG_012129.1:g.51090_51091delinsGT
NG_012129.2:g.51090_51091delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1445-24_1445-23delinsGT (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-24_1445-23delins...
ENST00000200652.3:c.1445-24_1445-23delinsGT (SLC22A4)	ENSP00000200652.3:n.1445-24_1445-23delins...
NM_003059.2:c.1445-24_1445-23delinsGT (SLC22A4)	NP_003050.2:n.1445-24_1445-23delinsGT
NR_110997.1:n.561-5616_561-5615delinsAC (MIR3936HG)
XM_006714675.2:c.917-24_917-23delinsGT (SLC22A4)	XP_006714738.1:n.917-24_917-23delinsGT
XM_011543589.1:c.1169-24_1169-23delinsGT (SLC22A4)	XP_011541891.1:n.1169-24_1169-23delinsGT
XM_006714675.4:c.917-24_917-23delinsGT (SLC22A4)	XP_006714738.1:n.917-24_917-23delinsGT
XM_011543589.2:c.1169-24_1169-23delinsGT (SLC22A4)	XP_011541891.1:n.1169-24_1169-23delinsGT
XM_017009776.1:c.917-24_917-23delinsGT (SLC22A4)	XP_016865265.1:n.917-24_917-23delinsGT
NM_003059.3:c.1445-24_1445-23delinsGT (SLC22A4) MANE Select	NP_003050.2:n.1445-24_1445-23delinsGT