Canonical Allele Identifier: CA1610179885
Gene: SYCP2L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897297A= , CM000668.2:g.10897297A= GRCh38
NC_000006.11:g.10897530A= , CM000668.1:g.10897530A= GRCh37
NC_000006.10:g.11005516A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-714A= MANE Select ENSP00000283141.6:n.337-714A=
ENST00000283141.10:c.337-714A= ENSP00000283141.6:n.337-714A=
ENST00000341041.8:c.337-714A= ENSP00000340320.4:n.337-714A=
ENST00000480294.1:c.*299-714A= ENSP00000417929.1:n.*299-714A=
ENST00000543878.5:c.334-714A= ENSP00000440676.2:n.334-714A=
NM_001040274.2:c.337-714A= NP_001035364.2:n.337-714A=
NM_001040274.3:c.337-714A= MANE Select NP_001035364.2:n.337-714A=