Canonical Allele Identifier: CA571549577

Gene: SLC22A3

Linked Data

• dbSNP Id: rs1270526539
• gnomAD v2: 6-160840199-A-AT
• gnomAD v3: 6-160419167-A-AT
• gnomAD v4: 6-160419167-A-AT
• MyVariant Identifiers: chr6:g.160840199_160840200insT (hg19) ; chr6:g.160419167_160419168insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160419175dup , CM000668.2:g.160419175dup	GRCh38
NC_000006.11:g.160840207dup , CM000668.1:g.160840207dup	GRCh37
NC_000006.10:g.160760197dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000275300.3:c.975+8329dup MANE Select	ENSP00000275300.2:n.975+8329dup
ENST00000275300.2:c.975+8329dup	ENSP00000275300.2:n.975+8329dup
NM_021977.3:c.975+8329dup	NP_068812.1:n.975+8329dup
XM_005267106.3:c.582+8329dup	XP_005267163.1:n.582+8329dup
XM_005267107.2:c.976-6676dup	XP_005267164.1:n.976-6676dup
XM_011536075.1:c.519+8329dup	XP_011534377.1:n.519+8329dup
XM_011536076.1:c.519+8329dup	XP_011534378.1:n.519+8329dup
XM_011536077.1:c.519+8329dup	XP_011534379.1:n.519+8329dup
XM_011536078.1:c.975+8329dup	XP_011534380.1:n.975+8329dup
XR_245546.1:n.1017+8329dup
XM_005267106.5:c.582+8329dup	XP_005267163.1:n.582+8329dup
XM_005267107.3:c.976-6676dup	XP_005267164.1:n.976-6676dup
XM_011536075.2:c.519+8329dup	XP_011534377.1:n.519+8329dup
XM_011536076.3:c.519+8329dup	XP_011534378.1:n.519+8329dup
XM_017011203.2:c.519+8329dup	XP_016866692.1:n.519+8329dup
XR_001743588.1:n.1017+8329dup
XR_001743589.1:n.1017+8329dup
NM_021977.4:c.975+8329dup MANE Select	NP_068812.1:n.975+8329dup