Canonical Allele Identifier: CA1640576

Gene: SLC3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44312651C>T , CM000664.2:g.44312651C>T	GRCh38
NC_000002.11:g.44539790C>T , CM000664.1:g.44539790C>T	GRCh37
NC_000002.10:g.44393294C>T	NCBI36
NG_008233.1:g.42194C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000341.4:c.1398C>T MANE Select	NP_000332.2:p.Asn466=
ENST00000260649.11:c.1398C>T MANE Select	ENSP00000260649.6:p.Asn466=
NM_000341.3:c.1398C>T	NP_000332.2:p.Asn466=
ENST00000260649.10:c.1398C>T	ENSP00000260649.6:p.Asn466=
ENST00000409229.7:c.1398C>T	ENSP00000386620.3:p.Asn466=
ENST00000409294.5:c.258C>T	ENSP00000386852.1:p.Asn86=
ENST00000409380.5:c.564C>T	ENSP00000386709.1:p.Asn188=
ENST00000409387.5:c.1398C>T	ENSP00000387308.1:p.Asn466=
ENST00000409740.3:c.291C>T	ENSP00000386677.3:p.Asn97=
ENST00000409741.5:c.1398C>T	ENSP00000386954.1:p.Asn466=
ENST00000611973.4:c.1398C>T	ENSP00000483618.1:p.Asn466=
ENST00000649044.1:c.*1409C>T	ENSP00000497083.1:n.*1409C>T
XM_011533047.1:c.1398C>T	XP_011531349.1:p.Asn466=
XM_011533047.3:c.1398C>T	XP_011531349.1:p.Asn466=