Canonical Allele Identifier: CA134131364

Gene: SYCP2L

Linked Data

• dbSNP Id: rs1008357202
• gnomAD v3: 6-10921222-A-G
• gnomAD v4: 6-10921222-A-G
• MyVariant Identifiers: chr6:g.10921455A>G (hg19) ; chr6:g.10921222A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10921222A>G , CM000668.2:g.10921222A>G	GRCh38
NC_000006.11:g.10921455A>G , CM000668.1:g.10921455A>G	GRCh37
NC_000006.10:g.11029441A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000283141.11:c.1073-3274A>G MANE Select	ENSP00000283141.6:n.1073-3274A>G
ENST00000283141.10:c.1073-3274A>G	ENSP00000283141.6:n.1073-3274A>G
ENST00000341041.8:c.*151-1469A>G	ENSP00000340320.4:n.*151-1469A>G
ENST00000480294.1:c.*1035-3274A>G	ENSP00000417929.1:n.*1035-3274A>G
ENST00000487561.2:c.556-3274A>G	ENSP00000417870.1:n.556-3274A>G
ENST00000543878.5:c.1070-3274A>G	ENSP00000440676.2:n.1070-3274A>G
NM_001040274.2:c.1073-3274A>G	NP_001035364.2:n.1073-3274A>G
NM_001040274.3:c.1073-3274A>G MANE Select	NP_001035364.2:n.1073-3274A>G