Canonical Allele Identifier: CA366345956

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160858121T>C (hg19) ; chr6:g.160437089T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437089T>C , CM000668.2:g.160437089T>C	GRCh38
NC_000006.11:g.160858121T>C , CM000668.1:g.160858121T>C	GRCh37
NC_000006.10:g.160778111T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1166T>C MANE Select	ENSP00000275300.2:p.Val389Ala
ENST00000275300.2:c.1166T>C	ENSP00000275300.2:p.Val389Ala
NM_021977.3:c.1166T>C	NP_068812.1:p.Val389Ala
XM_005267106.3:c.773T>C	XP_005267163.1:p.Val258Ala
XM_011536075.1:c.710T>C	XP_011534377.1:p.Val237Ala
XM_011536076.1:c.710T>C	XP_011534378.1:p.Val237Ala
XM_011536077.1:c.710T>C	XP_011534379.1:p.Val237Ala
XR_245546.1:n.1018-5672T>C
XM_005267106.5:c.773T>C	XP_005267163.1:p.Val258Ala
XM_011536075.2:c.710T>C	XP_011534377.1:p.Val237Ala
XM_011536076.3:c.710T>C	XP_011534378.1:p.Val237Ala
XM_017011203.2:c.710T>C	XP_016866692.1:p.Val237Ala
XR_001743588.1:n.1110T>C
XR_001743589.1:n.1018-5672T>C
NM_021977.4:c.1166T>C MANE Select	NP_068812.1:p.Val389Ala