Canonical Allele Identifier: CA238507361
Gene: LYZ HGNC NCBI

Linked Data

dbSNP Id: rs772760088
MyVariant Identifiers: chr12:g.69747459_69747460del (hg19) chr12:g.69353679_69353680del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.69353679_69353680del , CM000674.2:g.69353679_69353680del GRCh38
NC_000012.11:g.69747459_69747460del , CM000674.1:g.69747459_69747460del GRCh37
NC_000012.10:g.68033726_68033727del NCBI36
NG_008195.1:g.10326_10327del , LRG_768:g.10326_10327del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261267.7:c.*460_*461del MANE Select ENSP00000261267.2:n.*460_*461del
ENST00000261267.6:c.*460_*461del ENSP00000261267.2:n.*460_*461del
NM_000239.2:c.*460_*461del , LRG_768t1:c.*460_*461del NP_000230.1:n.*460_*461del
NM_000239.3:c.*460_*461del MANE Select NP_000230.1:n.*460_*461del
Search 100 bp 5'
Search 100 bp 3'