Canonical Allele Identifier: CA453047566

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160858071G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160437039G>C , CM000668.2:g.160437039G>C	GRCh38
NC_000006.11:g.160858071G>C , CM000668.1:g.160858071G>C	GRCh37
NC_000006.10:g.160778061G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1116G>C MANE Select	ENSP00000275300.2:p.Leu372=
ENST00000275300.2:c.1116G>C	ENSP00000275300.2:p.Leu372=
NM_021977.3:c.1116G>C	NP_068812.1:p.Leu372=
XM_005267106.3:c.723G>C	XP_005267163.1:p.Leu241=
XM_011536075.1:c.660G>C	XP_011534377.1:p.Leu220=
XM_011536076.1:c.660G>C	XP_011534378.1:p.Leu220=
XM_011536077.1:c.660G>C	XP_011534379.1:p.Leu220=
XR_245546.1:n.1018-5722G>C
XM_005267106.5:c.723G>C	XP_005267163.1:p.Leu241=
XM_011536075.2:c.660G>C	XP_011534377.1:p.Leu220=
XM_011536076.3:c.660G>C	XP_011534378.1:p.Leu220=
XM_017011203.2:c.660G>C	XP_016866692.1:p.Leu220=
XR_001743588.1:n.1060G>C
XR_001743589.1:n.1018-5722G>C
NM_021977.4:c.1116G>C MANE Select	NP_068812.1:p.Leu372=