Canonical Allele Identifier: CA623841760

Gene: SLC38A8

Linked Data

• dbSNP Id: rs1567700895
• gnomAD v2: 16-84065800-TTGTTG-T
• gnomAD v3: 16-84032195-TTGTTG-T
• gnomAD v4: 16-84032195-TTGTTG-T
• MyVariant Identifiers: chr16:g.84065801_84065805del (hg19) ; chr16:g.84032196_84032200del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.84032197_84032201del , CM000678.2:g.84032197_84032201del	GRCh38
NC_000016.9:g.84065802_84065806del , CM000678.1:g.84065802_84065806del	GRCh37
NC_000016.8:g.82623303_82623307del	NCBI36
NG_034136.1:g.14958_14962del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299709.8:c.531-232_531-228del MANE Select	ENSP00000299709.3:n.531-232_531-228del
ENST00000299709.7:c.531-232_531-228del	ENSP00000299709.3:n.531-232_531-228del
ENST00000568178.1:c.531-232_531-228del	ENSP00000457737.1:n.531-232_531-228del
NM_001080442.2:c.531-232_531-228del	NP_001073911.1:n.531-232_531-228del
XM_011522872.1:c.531-232_531-228del	XP_011521174.1:n.531-232_531-228del
XM_017022946.1:c.531-232_531-228del	XP_016878435.1:n.531-232_531-228del
NM_001080442.3:c.531-232_531-228del MANE Select	NP_001073911.1:n.531-232_531-228del