Canonical Allele Identifier: CA1583124986

Gene: SLC22A4 MIR3936HG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340530_132340531delinsAT , CM000667.2:g.132340530_132340531delinsAT	GRCh38
NC_000005.9:g.131676223_131676224delinsAT , CM000667.1:g.131676223_131676224delinsAT	GRCh37
NC_000005.8:g.131704122_131704123delinsAT	NCBI36
NG_012129.1:g.51079_51080delinsAT
NG_012129.2:g.51079_51080delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1445-35_1445-34delinsAT (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-35_1445-34delins...
ENST00000200652.3:c.1445-35_1445-34delinsAT (SLC22A4)	ENSP00000200652.3:n.1445-35_1445-34delins...
NM_003059.2:c.1445-35_1445-34delinsAT (SLC22A4)	NP_003050.2:n.1445-35_1445-34delinsAT
NR_110997.1:n.561-5605_561-5604delinsAT (MIR3936HG)
XM_006714675.2:c.917-35_917-34delinsAT (SLC22A4)	XP_006714738.1:n.917-35_917-34delinsAT
XM_011543589.1:c.1169-35_1169-34delinsAT (SLC22A4)	XP_011541891.1:n.1169-35_1169-34delinsAT
XM_006714675.4:c.917-35_917-34delinsAT (SLC22A4)	XP_006714738.1:n.917-35_917-34delinsAT
XM_011543589.2:c.1169-35_1169-34delinsAT (SLC22A4)	XP_011541891.1:n.1169-35_1169-34delinsAT
XM_017009776.1:c.917-35_917-34delinsAT (SLC22A4)	XP_016865265.1:n.917-35_917-34delinsAT
NM_003059.3:c.1445-35_1445-34delinsAT (SLC22A4) MANE Select	NP_003050.2:n.1445-35_1445-34delinsAT