Canonical Allele Identifier: CA2238382175

Gene: SLC38A8

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84031829_84031832delinsCCCG , CM000678.2:g.84031829_84031832delinsCCCG	GRCh38
NC_000016.9:g.84065434_84065437delinsCCCG , CM000678.1:g.84065434_84065437delinsCCCG	GRCh37
NC_000016.8:g.82622935_82622938delinsCCCG	NCBI36
NG_034136.1:g.15326_15329delinsCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.632+35_632+38delinsCGGG MANE Select	ENSP00000299709.3:n.632+35_632+38delinsCGGG
ENST00000299709.7:c.632+35_632+38delinsCGGG	ENSP00000299709.3:n.632+35_632+38delinsCGGG
ENST00000568178.1:c.632+35_632+38delinsCGGG	ENSP00000457737.1:n.632+35_632+38delinsCGGG
NM_001080442.2:c.632+35_632+38delinsCGGG	NP_001073911.1:n.632+35_632+38delinsCGGG
XM_011522872.1:c.632+35_632+38delinsCGGG	XP_011521174.1:n.632+35_632+38delinsCGGG
XM_017022946.1:c.632+35_632+38delinsCGGG	XP_016878435.1:n.632+35_632+38delinsCGGG
NM_001080442.3:c.632+35_632+38delinsCGGG MANE Select	NP_001073911.1:n.632+35_632+38delinsCGGG