Canonical Allele Identifier: CA565388172
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs57840245
gnomAD v2: 6-10897274-A-AT
gnomAD v3: 6-10897041-A-AT
gnomAD v4: 6-10897041-A-AT
MyVariant Identifiers: chr6:g.10897276_10897277insT (hg19) chr6:g.10897274_10897275insT (hg19) chr6:g.10897043_10897044insT (hg38) chr6:g.10897041_10897042insT (hg38)
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Genomic Alleles

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

Transcript Alleles

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