Canonical Allele Identifier: CA571906257

Gene: SLC22A3

Linked Data

• gnomAD v2: 6-160858206-A-AGGGGG
• MyVariant Identifiers: chr6:g.160858206_160858207insGGGGG (hg19) ; chr6:g.160437174_160437175insGGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437178_160437179insGGGGG , CM000668.2:g.160437178_160437179insGGGGG	GRCh38
NC_000006.11:g.160858210_160858211insGGGGG , CM000668.1:g.160858210_160858211insGGGGG	GRCh37
NC_000006.10:g.160778200_160778201insGGGGG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1255_1256insGGGGG MANE Select	ENSP00000275300.2:p.Val419GlyfsTer15
ENST00000275300.2:c.1255_1256insGGGGG	ENSP00000275300.2:p.Val419GlyfsTer15
NM_021977.3:c.1255_1256insGGGGG	NP_068812.1:p.Val419GlyfsTer15
XM_005267106.3:c.862_863insGGGGG	XP_005267163.1:p.Val288GlyfsTer15
XM_011536075.1:c.799_800insGGGGG	XP_011534377.1:p.Val267GlyfsTer15
XM_011536076.1:c.799_800insGGGGG	XP_011534378.1:p.Val267GlyfsTer15
XM_011536077.1:c.799_800insGGGGG	XP_011534379.1:p.Val267GlyfsTer15
XR_245546.1:n.1018-5583_1018-5582insGGGGG
XM_005267106.5:c.862_863insGGGGG	XP_005267163.1:p.Val288GlyfsTer15
XM_011536075.2:c.799_800insGGGGG	XP_011534377.1:p.Val267GlyfsTer15
XM_011536076.3:c.799_800insGGGGG	XP_011534378.1:p.Val267GlyfsTer15
XM_017011203.2:c.799_800insGGGGG	XP_016866692.1:p.Val267GlyfsTer15
XR_001743588.1:n.1199_1200insGGGGG
XR_001743589.1:n.1018-5583_1018-5582insGGGGG
NM_021977.4:c.1255_1256insGGGGG MANE Select	NP_068812.1:p.Val419GlyfsTer15