Canonical Allele Identifier: CA2675193387

Gene: SLC22A4 MIR3936HG

Linked Data

• gnomAD v4: 5-132340573-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132340573_132340574insC , CM000667.2:g.132340573_132340574insC	GRCh38
NC_000005.9:g.131676266_131676267insC , CM000667.1:g.131676266_131676267insC	GRCh37
NC_000005.8:g.131704165_131704166insC	NCBI36
NG_012129.1:g.51122_51123insC
NG_012129.2:g.51122_51123insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000200652.4:c.1453_1454insC (SLC22A4) MANE Select	ENSP00000200652.3:p.Asn485ThrfsTer11
ENST00000200652.3:c.1453_1454insC (SLC22A4)	ENSP00000200652.3:p.Asn485ThrfsTer11
NM_003059.2:c.1453_1454insC (SLC22A4)	NP_003050.2:p.Asn485ThrfsTer11
NR_110997.1:n.561-5648_561-5647insG (MIR3936HG)
XM_006714675.2:c.925_926insC (SLC22A4)	XP_006714738.1:p.Asn309ThrfsTer11
XM_011543589.1:c.1177_1178insC (SLC22A4)	XP_011541891.1:p.Asn393ThrfsTer11
XM_006714675.4:c.925_926insC (SLC22A4)	XP_006714738.1:p.Asn309ThrfsTer11
XM_011543589.2:c.1177_1178insC (SLC22A4)	XP_011541891.1:p.Asn393ThrfsTer11
XM_017009776.1:c.925_926insC (SLC22A4)	XP_016865265.1:p.Asn309ThrfsTer11
NM_003059.3:c.1453_1454insC (SLC22A4) MANE Select	NP_003050.2:p.Asn485ThrfsTer11