Canonical Allele Identifier: CA3720127
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs771907268
ExAC: 6:31687015 GT / G
gnomAD v2: 6-31687015-GT-G
gnomAD v3: 6-31719238-GT-G
gnomAD v4: 6-31719238-GT-G
MyVariant Identifiers: chr6:g.31687016del (hg19) chr6:g.31719239del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719241del , CM000668.2:g.31719241del GRCh38
NC_000006.11:g.31687018del , CM000668.1:g.31687018del GRCh37
NC_000006.10:g.31794997del NCBI36
NG_029044.1:g.898del
NG_029044.2:g.898del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.235del (LY6G6C) MANE Select ENSP00000364978.2:p.Thr79ProfsTer7
ENST00000375819.2:c.235del (LY6G6C) ENSP00000364978.2:p.Thr79ProfsTer7
ENST00000460663.5:n.90+558del (MPIG6B)
ENST00000495859.1:c.67del (LY6G6C) ENSP00000433207.1:p.Thr23ProfsTer7
NM_025261.2:c.235del (LY6G6C) NP_079537.1:p.Thr79ProfsTer7
NM_025261.3:c.235del (LY6G6C) MANE Select NP_079537.1:p.Thr79ProfsTer7
Search 100 bp 5'
Search 100 bp 3'