Canonical Allele Identifier: CA46490749

Gene: SLC3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44281042C>T , CM000664.2:g.44281042C>T	GRCh38
NC_000002.11:g.44508181C>T , CM000664.1:g.44508181C>T	GRCh37
NC_000002.10:g.44361685C>T	NCBI36
NG_008233.1:g.10585C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000341.4:c.610+147C>T MANE Select	NP_000332.2:n.610+147C>T
ENST00000260649.11:c.610+147C>T MANE Select	ENSP00000260649.6:n.610+147C>T
NM_000341.3:c.610+147C>T	NP_000332.2:n.610+147C>T
ENST00000260649.10:c.610+147C>T	ENSP00000260649.6:n.610+147C>T
ENST00000409229.7:c.610+147C>T	ENSP00000386620.3:n.610+147C>T
ENST00000409387.5:c.610+147C>T	ENSP00000387308.1:n.610+147C>T
ENST00000409741.5:c.610+147C>T	ENSP00000386954.1:n.610+147C>T
ENST00000410056.7:c.610+147C>T	ENSP00000387337.3:n.610+147C>T
ENST00000611973.4:c.610+147C>T	ENSP00000483618.1:n.610+147C>T
ENST00000649044.1:c.*621+147C>T	ENSP00000497083.1:n.*621+147C>T
XM_011533047.1:c.610+147C>T	XP_011531349.1:n.610+147C>T
XM_011533047.3:c.610+147C>T	XP_011531349.1:n.610+147C>T