Canonical Allele Identifier: CA1610219242
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921222_10921223delinsAT , CM000668.2:g.10921222_10921223delinsAT GRCh38
NC_000006.11:g.10921455_10921456delinsAT , CM000668.1:g.10921455_10921456delinsAT GRCh37
NC_000006.10:g.11029441_11029442delinsAT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3274_1073-3273delinsAT MANE Select ENSP00000283141.6:n.1073-3274_1073-3273de...
ENST00000283141.10:c.1073-3274_1073-3273delinsAT ENSP00000283141.6:n.1073-3274_1073-3273de...
ENST00000341041.8:c.*151-1469_*151-1468delinsAT ENSP00000340320.4:n.*151-1469_*151-1468de...
ENST00000480294.1:c.*1035-3274_*1035-3273delinsAT ENSP00000417929.1:n.*1035-3274_*1035-3273...
ENST00000487561.2:c.556-3274_556-3273delinsAT ENSP00000417870.1:n.556-3274_556-3273deli...
ENST00000543878.5:c.1070-3274_1070-3273delinsAT ENSP00000440676.2:n.1070-3274_1070-3273de...
NM_001040274.2:c.1073-3274_1073-3273delinsAT NP_001035364.2:n.1073-3274_1073-3273delin...
NM_001040274.3:c.1073-3274_1073-3273delinsAT MANE Select NP_001035364.2:n.1073-3274_1073-3273delin...