Canonical Allele Identifier: CA2238382209

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031872T= , CM000678.2:g.84031872T=	GRCh38
NC_000016.9:g.84065477T= , CM000678.1:g.84065477T=	GRCh37
NC_000016.8:g.82622978T=	NCBI36
NG_034136.1:g.15286A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.627A= MANE Select	ENSP00000299709.3:p.Ser209=
ENST00000299709.7:c.627A=	ENSP00000299709.3:p.Ser209=
ENST00000568178.1:c.627A=	ENSP00000457737.1:p.Ser209=
NM_001080442.2:c.627A=	NP_001073911.1:p.Ser209=
XM_011522872.1:c.627A=	XP_011521174.1:p.Ser209=
XM_017022946.1:c.627A=	XP_016878435.1:p.Ser209=
NM_001080442.3:c.627A= MANE Select	NP_001073911.1:p.Ser209=