Canonical Allele Identifier: CA448564688
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs1275939795
gnomAD v2: 6-10897642-TC-T
gnomAD v3: 6-10897409-TC-T
gnomAD v4: 6-10897409-TC-T
MyVariant Identifiers: chr6:g.10897643del (hg19) chr6:g.10897410del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897410del , CM000668.2:g.10897410del GRCh38
NC_000006.11:g.10897643del , CM000668.1:g.10897643del GRCh37
NC_000006.10:g.11005629del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000283141.11:c.337-601del MANE Select ENSP00000283141.6:n.337-601del
ENST00000283141.10:c.337-601del ENSP00000283141.6:n.337-601del
ENST00000341041.8:c.337-601del ENSP00000340320.4:n.337-601del
ENST00000480294.1:c.*299-601del ENSP00000417929.1:n.*299-601del
ENST00000543878.5:c.334-601del ENSP00000440676.2:n.334-601del
NM_001040274.2:c.337-601del NP_001035364.2:n.337-601del
NM_001040274.3:c.337-601del MANE Select NP_001035364.2:n.337-601del
Search 100 bp 5'
Search 100 bp 3'