Canonical Allele Identifier: CA366345707

Gene: SLC22A3

Linked Data

• MyVariant Identifiers: chr6:g.160857893A>C (hg19) ; chr6:g.160436861A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.160436861A>C , CM000668.2:g.160436861A>C	GRCh38
NC_000006.11:g.160857893A>C , CM000668.1:g.160857893A>C	GRCh37
NC_000006.10:g.160777883A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000275300.3:c.1057A>C MANE Select	ENSP00000275300.2:p.Ile353Leu
ENST00000275300.2:c.1057A>C	ENSP00000275300.2:p.Ile353Leu
NM_021977.3:c.1057A>C	NP_068812.1:p.Ile353Leu
XM_005267106.3:c.664A>C	XP_005267163.1:p.Ile222Leu
XM_011536075.1:c.601A>C	XP_011534377.1:p.Ile201Leu
XM_011536076.1:c.601A>C	XP_011534378.1:p.Ile201Leu
XM_011536077.1:c.601A>C	XP_011534379.1:p.Ile201Leu
XR_245546.1:n.1018-5900A>C
XM_005267106.5:c.664A>C	XP_005267163.1:p.Ile222Leu
XM_011536075.2:c.601A>C	XP_011534377.1:p.Ile201Leu
XM_011536076.3:c.601A>C	XP_011534378.1:p.Ile201Leu
XM_017011203.2:c.601A>C	XP_016866692.1:p.Ile201Leu
XR_001743588.1:n.1018-136A>C
XR_001743589.1:n.1018-5900A>C
NM_021977.4:c.1057A>C MANE Select	NP_068812.1:p.Ile353Leu