Canonical Allele Identifier: CA2238382207

Gene: SLC38A8

Linked Data

• dbSNP Id: rs2085243604

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031870dup , CM000678.2:g.84031870dup	GRCh38
NC_000016.9:g.84065475dup , CM000678.1:g.84065475dup	GRCh37
NC_000016.8:g.82622976dup	NCBI36
NG_034136.1:g.15288dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.629dup MANE Select	ENSP00000299709.3:p.Ser211GlufsTer?
ENST00000299709.7:c.629dup	ENSP00000299709.3:p.Ser211GlufsTer?
ENST00000568178.1:c.629dup	ENSP00000457737.1:p.Ser211GlufsTer?
NM_001080442.2:c.629dup	NP_001073911.1:p.Ser211GlufsTer?
XM_011522872.1:c.629dup	XP_011521174.1:p.Ser211GlufsTer?
XM_017022946.1:c.629dup	XP_016878435.1:p.Ser211GlufsTer?
NM_001080442.3:c.629dup MANE Select	NP_001073911.1:p.Ser211GlufsTer?