Canonical Allele Identifier: CA2675193385

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132340564-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340564_132340565insA , CM000667.2:g.132340564_132340565insA	GRCh38
NC_000005.9:g.131676257_131676258insA , CM000667.1:g.131676257_131676258insA	GRCh37
NC_000005.8:g.131704156_131704157insA	NCBI36
NG_012129.1:g.51113_51114insA
NG_012129.2:g.51113_51114insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1445-1_1445insA (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-1_1445insA
ENST00000200652.3:c.1445-1_1445insA (SLC22A4)	ENSP00000200652.3:n.1445-1_1445insA
NM_003059.2:c.1445-1_1445insA (SLC22A4)	NP_003050.2:n.1445-1_1445insA
NR_110997.1:n.561-5639_561-5638insT (MIR3936HG)
XM_006714675.2:c.917-1_917insA (SLC22A4)	XP_006714738.1:n.917-1_917insA
XM_011543589.1:c.1169-1_1169insA (SLC22A4)	XP_011541891.1:n.1169-1_1169insA
XM_006714675.4:c.917-1_917insA (SLC22A4)	XP_006714738.1:n.917-1_917insA
XM_011543589.2:c.1169-1_1169insA (SLC22A4)	XP_011541891.1:n.1169-1_1169insA
XM_017009776.1:c.917-1_917insA (SLC22A4)	XP_016865265.1:n.917-1_917insA
NM_003059.3:c.1445-1_1445insA (SLC22A4) MANE Select	NP_003050.2:n.1445-1_1445insA