Canonical Allele Identifier: CA16254067
Gene: SYCP2L HGNC NCBI

Linked Data

dbSNP Id: rs2153157

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10897255G>A , CM000668.2:g.10897255G>A GRCh38
NC_000006.11:g.10897488G>A , CM000668.1:g.10897488G>A GRCh37
NC_000006.10:g.11005474G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000283141.11:c.337-756G>A MANE Select ENSP00000283141.6:n.337-756G>A
ENST00000283141.10:c.337-756G>A ENSP00000283141.6:n.337-756G>A
ENST00000341041.8:c.337-756G>A ENSP00000340320.4:n.337-756G>A
ENST00000480294.1:c.*299-756G>A ENSP00000417929.1:n.*299-756G>A
ENST00000543878.5:n.334-756G>A ENSP00000440676.2:n.334-756G>A
NM_001040274.2:c.337-756G>A NP_001035364.2:n.337-756G>A
NM_001040274.3:c.337-756G>A MANE Select NP_001035364.2:n.337-756G>A