Canonical Allele Identifier: CA2580066535

Gene: SLC3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44286161A>G , CM000664.2:g.44286161A>G	GRCh38
NC_000002.11:g.44513300A>G , CM000664.1:g.44513300A>G	GRCh37
NC_000002.10:g.44366804A>G	NCBI36
NG_008233.1:g.15704A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000341.4:c.891+4A>G MANE Select	NP_000332.2:n.891+4A>G
ENST00000260649.11:c.891+4A>G MANE Select	ENSP00000260649.6:n.891+4A>G
NM_000341.3:c.891+4A>G	NP_000332.2:n.891+4A>G
ENST00000260649.10:c.891+4A>G	ENSP00000260649.6:n.891+4A>G
ENST00000409229.7:c.891+4A>G	ENSP00000386620.3:n.891+4A>G
ENST00000409380.5:c.57+4A>G	ENSP00000386709.1:n.57+4A>G
ENST00000409387.5:c.891+4A>G	ENSP00000387308.1:n.891+4A>G
ENST00000409741.5:c.891+4A>G	ENSP00000386954.1:n.891+4A>G
ENST00000410056.7:c.891+4A>G	ENSP00000387337.3:n.891+4A>G
ENST00000427285.1:c.225+4A>G	ENSP00000391642.1:n.225+4A>G
ENST00000611973.4:c.891+4A>G	ENSP00000483618.1:n.891+4A>G
ENST00000649044.1:c.*902+4A>G	ENSP00000497083.1:n.*902+4A>G
XM_011533047.1:c.891+4A>G	XP_011531349.1:n.891+4A>G
XM_011533047.3:c.891+4A>G	XP_011531349.1:n.891+4A>G