Canonical Allele Identifier: CA2675193386

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132340572-C-CCCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340572_132340573insCCTT , CM000667.2:g.132340572_132340573insCCTT	GRCh38
NC_000005.9:g.131676265_131676266insCCTT , CM000667.1:g.131676265_131676266insCCTT	GRCh37
NC_000005.8:g.131704164_131704165insCCTT	NCBI36
NG_012129.1:g.51121_51122insCCTT
NG_012129.2:g.51121_51122insCCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1452_1453insCCTT (SLC22A4) MANE Select	ENSP00000200652.3:p.Asn485ProfsTer2
ENST00000200652.3:c.1452_1453insCCTT (SLC22A4)	ENSP00000200652.3:p.Asn485ProfsTer2
NM_003059.2:c.1452_1453insCCTT (SLC22A4)	NP_003050.2:p.Asn485ProfsTer2
NR_110997.1:n.561-5647_561-5646insAAGG (MIR3936HG)
XM_006714675.2:c.924_925insCCTT (SLC22A4)	XP_006714738.1:p.Asn309ProfsTer2
XM_011543589.1:c.1176_1177insCCTT (SLC22A4)	XP_011541891.1:p.Asn393ProfsTer2
XM_006714675.4:c.924_925insCCTT (SLC22A4)	XP_006714738.1:p.Asn309ProfsTer2
XM_011543589.2:c.1176_1177insCCTT (SLC22A4)	XP_011541891.1:p.Asn393ProfsTer2
XM_017009776.1:c.924_925insCCTT (SLC22A4)	XP_016865265.1:p.Asn309ProfsTer2
NM_003059.3:c.1452_1453insCCTT (SLC22A4) MANE Select	NP_003050.2:p.Asn485ProfsTer2