Canonical Allele Identifier: CA1610219211
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921212_10921213delinsCA , CM000668.2:g.10921212_10921213delinsCA GRCh38
NC_000006.11:g.10921445_10921446delinsCA , CM000668.1:g.10921445_10921446delinsCA GRCh37
NC_000006.10:g.11029431_11029432delinsCA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3284_1073-3283delinsCA MANE Select ENSP00000283141.6:n.1073-3284_1073-3283de...
ENST00000283141.10:c.1073-3284_1073-3283delinsCA ENSP00000283141.6:n.1073-3284_1073-3283de...
ENST00000341041.8:c.*151-1479_*151-1478delinsCA ENSP00000340320.4:n.*151-1479_*151-1478de...
ENST00000480294.1:c.*1035-3284_*1035-3283delinsCA ENSP00000417929.1:n.*1035-3284_*1035-3283...
ENST00000487561.2:c.556-3284_556-3283delinsCA ENSP00000417870.1:n.556-3284_556-3283deli...
ENST00000543878.5:c.1070-3284_1070-3283delinsCA ENSP00000440676.2:n.1070-3284_1070-3283de...
NM_001040274.2:c.1073-3284_1073-3283delinsCA NP_001035364.2:n.1073-3284_1073-3283delin...
NM_001040274.3:c.1073-3284_1073-3283delinsCA MANE Select NP_001035364.2:n.1073-3284_1073-3283delin...