Canonical Allele Identifier: CA1640430

Gene: SLC3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44301137G>A , CM000664.2:g.44301137G>A	GRCh38
NC_000002.11:g.44528276G>A , CM000664.1:g.44528276G>A	GRCh37
NC_000002.10:g.44381780G>A	NCBI36
NG_008233.1:g.30680G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000341.4:c.1136+10G>A MANE Select	NP_000332.2:n.1136+10G>A
ENST00000260649.11:c.1136+10G>A MANE Select	ENSP00000260649.6:n.1136+10G>A
NM_000341.3:c.1136+10G>A	NP_000332.2:n.1136+10G>A
ENST00000260649.10:c.1136+10G>A	ENSP00000260649.6:n.1136+10G>A
ENST00000409229.7:c.1136+10G>A	ENSP00000386620.3:n.1136+10G>A
ENST00000409294.5:c.-5+1047G>A	ENSP00000386852.1:n.-5+1047G>A
ENST00000409380.5:c.302+10G>A	ENSP00000386709.1:n.302+10G>A
ENST00000409387.5:c.1136+10G>A	ENSP00000387308.1:n.1136+10G>A
ENST00000409741.5:c.1136+10G>A	ENSP00000386954.1:n.1136+10G>A
ENST00000410056.7:c.1146G>A	ENSP00000387337.3:p.Thr382=
ENST00000611973.4:c.1136+10G>A	ENSP00000483618.1:n.1136+10G>A
ENST00000649044.1:c.*1147+10G>A	ENSP00000497083.1:n.*1147+10G>A
XM_011533047.1:c.1136+10G>A	XP_011531349.1:n.1136+10G>A
XM_011533047.3:c.1136+10G>A	XP_011531349.1:n.1136+10G>A