Canonical Allele Identifier: CA13603938

Gene: KSR2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117517222G>T , CM000674.2:g.117517222G>T	GRCh38
NC_000012.11:g.117955027G>T , CM000674.1:g.117955027G>T	GRCh37
NC_000012.10:g.116439410G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.2219+7630C>A MANE Select	ENSP00000339952.4:n.2219+7630C>A
ENST00000339824.6:c.2219+7630C>A	ENSP00000339952.4:n.2219+7630C>A
ENST00000425217.5:c.2132+7630C>A	ENSP00000389715.1:n.2132+7630C>A
NM_173598.4:c.2132+7630C>A	NP_775869.3:n.2132+7630C>A
XM_011538224.1:c.2213+7630C>A	XP_011536526.1:n.2213+7630C>A
XM_011538225.1:c.1856+7630C>A	XP_011536527.1:n.1856+7630C>A
XM_011538227.1:c.1355+7630C>A	XP_011536529.1:n.1355+7630C>A
XM_011538228.1:c.1310+7630C>A	XP_011536530.1:n.1310+7630C>A
XM_011538230.1:c.959+7630C>A	XP_011536532.1:n.959+7630C>A
XR_944522.1:n.3053+7630C>A
XM_011538224.3:c.2213+7630C>A	XP_011536526.1:n.2213+7630C>A
XM_011538225.3:c.1856+7630C>A	XP_011536527.1:n.1856+7630C>A
XM_017019208.2:c.2219+7630C>A	XP_016874697.1:n.2219+7630C>A
XM_017019210.2:c.914+7630C>A	XP_016874699.1:n.914+7630C>A
NM_173598.6:c.2219+7630C>A MANE Select	NP_775869.4:n.2219+7630C>A