Canonical Allele Identifier: CA952330043
Gene: KSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1895160846

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117916058del , CM000674.2:g.117916058del GRCh38
NC_000012.11:g.118353863del , CM000674.1:g.118353863del GRCh37
NC_000012.10:g.116838246del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339824.7:c.180+52018del MANE Select ENSP00000339952.4:n.180+52018del
ENST00000339824.6:c.180+52018del ENSP00000339952.4:n.180+52018del
ENST00000425217.5:c.93+52018del ENSP00000389715.1:n.93+52018del
NM_173598.4:c.93+52018del NP_775869.3:n.93+52018del
XM_011538224.1:c.180+52018del XP_011536526.1:n.180+52018del
XM_011538226.1:c.180+52018del XP_011536528.1:n.180+52018del
XM_011538229.1:c.180+52018del XP_011536531.1:n.180+52018del
XR_944522.1:n.1014+52018del
XM_011538224.3:c.180+52018del XP_011536526.1:n.180+52018del
XM_011538226.3:c.180+52018del XP_011536528.1:n.180+52018del
XM_011538229.3:c.180+52018del XP_011536531.1:n.180+52018del
XM_017019208.2:c.180+52018del XP_016874697.1:n.180+52018del
XM_017019209.2:c.180+52018del XP_016874698.1:n.180+52018del
NM_173598.6:c.180+52018del MANE Select NP_775869.4:n.180+52018del