Canonical Allele Identifier: CA562764483

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1247858889
• gnomAD v2: 5-131676090-T-TA
• gnomAD v3: 5-132340397-T-TA
• gnomAD v4: 5-132340397-T-TA
• MyVariant Identifiers: chr5:g.131676090_131676091insA (hg19) ; chr5:g.132340397_132340398insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340397_132340398insA , CM000667.2:g.132340397_132340398insA	GRCh38
NC_000005.9:g.131676090_131676091insA , CM000667.1:g.131676090_131676091insA	GRCh37
NC_000005.8:g.131703989_131703990insA	NCBI36
NG_012129.1:g.50946_50947insA
NG_012129.2:g.50946_50947insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1445-168_1445-167insA (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-168_1445-167insA
ENST00000200652.3:c.1445-168_1445-167insA (SLC22A4)	ENSP00000200652.3:n.1445-168_1445-167insA
NM_003059.2:c.1445-168_1445-167insA (SLC22A4)	NP_003050.2:n.1445-168_1445-167insA
NR_110997.1:n.561-5472_561-5471insT (MIR3936HG)
XM_006714675.2:c.917-168_917-167insA (SLC22A4)	XP_006714738.1:n.917-168_917-167insA
XM_011543589.1:c.1169-168_1169-167insA (SLC22A4)	XP_011541891.1:n.1169-168_1169-167insA
XM_006714675.4:c.917-168_917-167insA (SLC22A4)	XP_006714738.1:n.917-168_917-167insA
XM_011543589.2:c.1169-168_1169-167insA (SLC22A4)	XP_011541891.1:n.1169-168_1169-167insA
XM_017009776.1:c.917-168_917-167insA (SLC22A4)	XP_016865265.1:n.917-168_917-167insA
NM_003059.3:c.1445-168_1445-167insA (SLC22A4) MANE Select	NP_003050.2:n.1445-168_1445-167insA