Canonical Allele Identifier: CA3720107
Gene: LY6G6C HGNC NCBI
MPIG6B HGNC NCBI

Linked Data

dbSNP Id: rs778588618
ExAC: 6:31686898 CCAGCCAAGGA / C
gnomAD v2: 6-31686898-CCAGCCAAGGA-C
gnomAD v4: 6-31719121-CCAGCCAAGGA-C
MyVariant Identifiers: chr6:g.31686899_31686908del (hg19) chr6:g.31719122_31719131del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31719122_31719131del , CM000668.2:g.31719122_31719131del GRCh38
NC_000006.11:g.31686899_31686908del , CM000668.1:g.31686899_31686908del GRCh37
NC_000006.10:g.31794878_31794887del NCBI36
NG_029044.1:g.779_788del
NG_029044.2:g.779_788del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375819.3:c.343_352del (LY6G6C) MANE Select ENSP00000364978.2:p.Ser115AlafsTer?
ENST00000375819.2:c.343_352del (LY6G6C) ENSP00000364978.2:p.Ser115AlafsTer?
ENST00000460663.5:n.90+439_90+448del (MPIG6B)
ENST00000495859.1:c.175_184del (LY6G6C) ENSP00000433207.1:p.Ser59AlafsTer?
NM_025261.2:c.343_352del (LY6G6C) NP_079537.1:p.Ser115AlafsTer?
NM_025261.3:c.343_352del (LY6G6C) MANE Select NP_079537.1:p.Ser115AlafsTer?
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