Canonical Allele Identifier: CA1677066970

Gene: SLC22A3

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160451620G>C , CM000668.2:g.160451620G>C	GRCh38
NC_000006.11:g.160872652G>C , CM000668.1:g.160872652G>C	GRCh37
NC_000006.10:g.160792642G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.*564G>C MANE Select	ENSP00000275300.2:n.*564G>C
ENST00000275300.2:c.*564G>C	ENSP00000275300.2:n.*564G>C
NM_021977.3:c.*564G>C	NP_068812.1:n.*564G>C
XM_005267106.3:c.*564G>C	XP_005267163.1:n.*564G>C
XM_011536075.1:c.*564G>C	XP_011534377.1:n.*564G>C
XM_011536076.1:c.*564G>C	XP_011534378.1:n.*564G>C
XM_011536077.1:c.*564G>C	XP_011534379.1:n.*564G>C
XM_005267106.5:c.*564G>C	XP_005267163.1:n.*564G>C
XM_011536075.2:c.*564G>C	XP_011534377.1:n.*564G>C
XM_011536076.3:c.*564G>C	XP_011534378.1:n.*564G>C
XM_017011203.2:c.*564G>C	XP_016866692.1:n.*564G>C
XR_001743588.1:n.2179G>C
XR_001743589.1:n.1964G>C
NM_021977.4:c.*564G>C MANE Select	NP_068812.1:n.*564G>C