Canonical Allele Identifier: CA562764484

Gene: SLC22A4 MIR3936HG

Linked Data

• dbSNP Id: rs1475359061
• gnomAD v2: 5-131676091-G-GACGGAGT
• gnomAD v3: 5-132340398-G-GACGGAGT
• gnomAD v4: 5-132340398-G-GACGGAGT
• MyVariant Identifiers: chr5:g.131676091_131676092insACGGAGT (hg19) ; chr5:g.132340398_132340399insACGGAGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340398_132340399insACGGAGT , CM000667.2:g.132340398_132340399insACGGAGT	GRCh38
NC_000005.9:g.131676091_131676092insACGGAGT , CM000667.1:g.131676091_131676092insACGGAGT	GRCh37
NC_000005.8:g.131703990_131703991insACGGAGT	NCBI36
NG_012129.1:g.50947_50948insACGGAGT
NG_012129.2:g.50947_50948insACGGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000200652.4:c.1445-167_1445-166insACGGAGT (SLC22A4) MANE Select	ENSP00000200652.3:n.1445-167_1445-166insACGGAGT
ENST00000200652.3:c.1445-167_1445-166insACGGAGT (SLC22A4)	ENSP00000200652.3:n.1445-167_1445-166insACGGAGT
NM_003059.2:c.1445-167_1445-166insACGGAGT (SLC22A4)	NP_003050.2:n.1445-167_1445-166insACGGAGT
NR_110997.1:n.561-5473_561-5472insACTCCGT (MIR3936HG)
XM_006714675.2:c.917-167_917-166insACGGAGT (SLC22A4)	XP_006714738.1:n.917-167_917-166insACGGAGT
XM_011543589.1:c.1169-167_1169-166insACGGAGT (SLC22A4)	XP_011541891.1:n.1169-167_1169-166insACGGAGT
XM_006714675.4:c.917-167_917-166insACGGAGT (SLC22A4)	XP_006714738.1:n.917-167_917-166insACGGAGT
XM_011543589.2:c.1169-167_1169-166insACGGAGT (SLC22A4)	XP_011541891.1:n.1169-167_1169-166insACGGAGT
XM_017009776.1:c.917-167_917-166insACGGAGT (SLC22A4)	XP_016865265.1:n.917-167_917-166insACGGAGT
NM_003059.3:c.1445-167_1445-166insACGGAGT (SLC22A4) MANE Select	NP_003050.2:n.1445-167_1445-166insACGGAGT