Canonical Allele Identifier: CA2494208443

Gene: SLC3A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44301076G= , CM000664.2:g.44301076G=	GRCh38
NC_000002.11:g.44528215G= , CM000664.1:g.44528215G=	GRCh37
NC_000002.10:g.44381719G=	NCBI36
NG_008233.1:g.30619G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260649.11:c.1085G= MANE Select	ENSP00000260649.6:p.Arg362=
ENST00000649044.1:c.*1096G=	ENSP00000497083.1:n.*1096G=
ENST00000260649.10:c.1085G=	ENSP00000260649.6:p.Arg362=
ENST00000409229.7:c.1085G=	ENSP00000386620.3:p.Arg362=
ENST00000409294.5:c.-5+986G=	ENSP00000386852.1:n.-5+986G=
ENST00000409380.5:c.251G=	ENSP00000386709.1:p.Arg84=
ENST00000409387.5:c.1085G=	ENSP00000387308.1:p.Arg362=
ENST00000409741.5:c.1085G=	ENSP00000386954.1:p.Arg362=
ENST00000410056.7:c.1085G=	ENSP00000387337.3:p.Arg362=
ENST00000427285.1:c.419G=	ENSP00000391642.1:p.Arg140=
ENST00000611973.4:c.1085G=	ENSP00000483618.1:p.Arg362=
NM_000341.3:c.1085G=	NP_000332.2:p.Arg362=
XM_011533047.1:c.1085G=	XP_011531349.1:p.Arg362=
XM_011533047.3:c.1085G=	XP_011531349.1:p.Arg362=
NM_000341.4:c.1085G= MANE Select	NP_000332.2:p.Arg362=