Canonical Allele Identifier: CA13603940
Gene: KSR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117518617C>T , CM000674.2:g.117518617C>T GRCh38
NC_000012.11:g.117956422C>T , CM000674.1:g.117956422C>T GRCh37
NC_000012.10:g.116440805C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339824.7:c.2219+6235G>A MANE Select ENSP00000339952.4:n.2219+6235G>A
ENST00000339824.6:c.2219+6235G>A ENSP00000339952.4:n.2219+6235G>A
ENST00000425217.5:c.2132+6235G>A ENSP00000389715.1:n.2132+6235G>A
ENST00000545002.1:n.1366-765G>A
NM_173598.4:c.2132+6235G>A NP_775869.3:n.2132+6235G>A
XM_011538224.1:c.2213+6235G>A XP_011536526.1:n.2213+6235G>A
XM_011538225.1:c.1856+6235G>A XP_011536527.1:n.1856+6235G>A
XM_011538226.1:c.2220-765G>A XP_011536528.1:n.2220-765G>A
XM_011538227.1:c.1355+6235G>A XP_011536529.1:n.1355+6235G>A
XM_011538228.1:c.1310+6235G>A XP_011536530.1:n.1310+6235G>A
XM_011538230.1:c.959+6235G>A XP_011536532.1:n.959+6235G>A
XR_944522.1:n.3053+6235G>A
XM_011538224.3:c.2213+6235G>A XP_011536526.1:n.2213+6235G>A
XM_011538225.3:c.1856+6235G>A XP_011536527.1:n.1856+6235G>A
XM_011538226.3:c.2220-765G>A XP_011536528.1:n.2220-765G>A
XM_017019208.2:c.2219+6235G>A XP_016874697.1:n.2219+6235G>A
XM_017019210.2:c.914+6235G>A XP_016874699.1:n.914+6235G>A
NM_173598.6:c.2219+6235G>A MANE Select NP_775869.4:n.2219+6235G>A
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