Canonical Allele Identifier: CA496764433

Gene: SLC38A8

Linked Data

• MyVariant Identifiers: chr16:g.84065531G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031926G>T , CM000678.2:g.84031926G>T	GRCh38
NC_000016.9:g.84065531G>T , CM000678.1:g.84065531G>T	GRCh37
NC_000016.8:g.82623032G>T	NCBI36
NG_034136.1:g.15232C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.573C>A MANE Select	ENSP00000299709.3:p.Ile191=
ENST00000299709.7:c.573C>A	ENSP00000299709.3:p.Ile191=
ENST00000568178.1:c.573C>A	ENSP00000457737.1:p.Ile191=
NM_001080442.2:c.573C>A	NP_001073911.1:p.Ile191=
XM_011522872.1:c.573C>A	XP_011521174.1:p.Ile191=
XM_017022946.1:c.573C>A	XP_016878435.1:p.Ile191=
NM_001080442.3:c.573C>A MANE Select	NP_001073911.1:p.Ile191=