Canonical Allele Identifier: CA1610219238
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10921221_10921222delinsTA , CM000668.2:g.10921221_10921222delinsTA GRCh38
NC_000006.11:g.10921454_10921455delinsTA , CM000668.1:g.10921454_10921455delinsTA GRCh37
NC_000006.10:g.11029440_11029441delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.1073-3275_1073-3274delinsTA MANE Select ENSP00000283141.6:n.1073-3275_1073-3274de...
ENST00000283141.10:c.1073-3275_1073-3274delinsTA ENSP00000283141.6:n.1073-3275_1073-3274de...
ENST00000341041.8:c.*151-1470_*151-1469delinsTA ENSP00000340320.4:n.*151-1470_*151-1469de...
ENST00000480294.1:c.*1035-3275_*1035-3274delinsTA ENSP00000417929.1:n.*1035-3275_*1035-3274...
ENST00000487561.2:c.556-3275_556-3274delinsTA ENSP00000417870.1:n.556-3275_556-3274deli...
ENST00000543878.5:c.1070-3275_1070-3274delinsTA ENSP00000440676.2:n.1070-3275_1070-3274de...
NM_001040274.2:c.1073-3275_1073-3274delinsTA NP_001035364.2:n.1073-3275_1073-3274delin...
NM_001040274.3:c.1073-3275_1073-3274delinsTA MANE Select NP_001035364.2:n.1073-3275_1073-3274delin...