Canonical Allele Identifier: CA607817221
Gene: KSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1324977802

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117916034C>G , CM000674.2:g.117916034C>G GRCh38
NC_000012.11:g.118353839C>G , CM000674.1:g.118353839C>G GRCh37
NC_000012.10:g.116838222C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339824.7:c.180+52042G>C MANE Select ENSP00000339952.4:n.180+52042G>C
ENST00000339824.6:c.180+52042G>C ENSP00000339952.4:n.180+52042G>C
ENST00000425217.5:c.93+52042G>C ENSP00000389715.1:n.93+52042G>C
NM_173598.4:c.93+52042G>C NP_775869.3:n.93+52042G>C
XM_011538224.1:c.180+52042G>C XP_011536526.1:n.180+52042G>C
XM_011538226.1:c.180+52042G>C XP_011536528.1:n.180+52042G>C
XM_011538229.1:c.180+52042G>C XP_011536531.1:n.180+52042G>C
XR_944522.1:n.1014+52042G>C
XM_011538224.3:c.180+52042G>C XP_011536526.1:n.180+52042G>C
XM_011538226.3:c.180+52042G>C XP_011536528.1:n.180+52042G>C
XM_011538229.3:c.180+52042G>C XP_011536531.1:n.180+52042G>C
XM_017019208.2:c.180+52042G>C XP_016874697.1:n.180+52042G>C
XM_017019209.2:c.180+52042G>C XP_016874698.1:n.180+52042G>C
NM_173598.6:c.180+52042G>C MANE Select NP_775869.4:n.180+52042G>C