Canonical Allele Identifier: CA134115005
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs57840245
gnomAD v2: 6-10897274-AT-A
gnomAD v3: 6-10897041-AT-A
gnomAD v4: 6-10897041-AT-A
MyVariant Identifiers: chr6:g.10897276del (hg19) chr6:g.10897275del (hg19) chr6:g.10897043del (hg38) chr6:g.10897042del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897052del , CM000668.2:g.10897052del GRCh38
NC_000006.11:g.10897285del , CM000668.1:g.10897285del GRCh37
NC_000006.10:g.11005271del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-959del MANE Select ENSP00000283141.6:n.337-959del
ENST00000283141.10:c.337-959del ENSP00000283141.6:n.337-959del
ENST00000341041.8:c.337-959del ENSP00000340320.4:n.337-959del
ENST00000480294.1:c.*299-959del ENSP00000417929.1:n.*299-959del
ENST00000543878.5:c.334-959del ENSP00000440676.2:n.334-959del
NM_001040274.2:c.337-959del NP_001035364.2:n.337-959del
NM_001040274.3:c.337-959del MANE Select NP_001035364.2:n.337-959del
Search 100 bp 5'
Search 100 bp 3'