Canonical Allele Identifier: CA496764436

Gene: SLC38A8

Linked Data

• MyVariant Identifiers: chr16:g.84065537C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031932C>A , CM000678.2:g.84031932C>A	GRCh38
NC_000016.9:g.84065537C>A , CM000678.1:g.84065537C>A	GRCh37
NC_000016.8:g.82623038C>A	NCBI36
NG_034136.1:g.15226G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.567G>T MANE Select	ENSP00000299709.3:p.Leu189=
ENST00000299709.7:c.567G>T	ENSP00000299709.3:p.Leu189=
ENST00000568178.1:c.567G>T	ENSP00000457737.1:p.Leu189=
NM_001080442.2:c.567G>T	NP_001073911.1:p.Leu189=
XM_011522872.1:c.567G>T	XP_011521174.1:p.Leu189=
XM_017022946.1:c.567G>T	XP_016878435.1:p.Leu189=
NM_001080442.3:c.567G>T MANE Select	NP_001073911.1:p.Leu189=