Canonical Allele Identifier: CA1085948012

Gene: SYCP2L

Linked Data

• dbSNP Id: rs1780273918
• gnomAD v3: 6-10897313-CT-C
• gnomAD v4: 6-10897313-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10897316del , CM000668.2:g.10897316del	GRCh38
NC_000006.11:g.10897549del , CM000668.1:g.10897549del	GRCh37
NC_000006.10:g.11005535del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.337-695del MANE Select	ENSP00000283141.6:n.337-695del
ENST00000283141.10:c.337-695del	ENSP00000283141.6:n.337-695del
ENST00000341041.8:c.337-695del	ENSP00000340320.4:n.337-695del
ENST00000480294.1:c.*299-695del	ENSP00000417929.1:n.*299-695del
ENST00000543878.5:c.334-695del	ENSP00000440676.2:n.334-695del
NM_001040274.2:c.337-695del	NP_001035364.2:n.337-695del
NM_001040274.3:c.337-695del MANE Select	NP_001035364.2:n.337-695del