Canonical Allele Identifier: CA13702676

Gene: KSR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117656262C>T , CM000674.2:g.117656262C>T	GRCh38
NC_000012.11:g.118094067C>T , CM000674.1:g.118094067C>T	GRCh37
NC_000012.10:g.116578450C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.1171+11212G>A MANE Select	ENSP00000339952.4:n.1171+11212G>A
ENST00000339824.6:c.1171+11212G>A	ENSP00000339952.4:n.1171+11212G>A
ENST00000425217.5:c.1084+11212G>A	ENSP00000389715.1:n.1084+11212G>A
ENST00000545002.1:n.317+11212G>A
NM_173598.4:c.1084+11212G>A	NP_775869.3:n.1084+11212G>A
XM_011538224.1:c.1171+11212G>A	XP_011536526.1:n.1171+11212G>A
XM_011538225.1:c.808+11212G>A	XP_011536527.1:n.808+11212G>A
XM_011538226.1:c.1171+11212G>A	XP_011536528.1:n.1171+11212G>A
XM_011538227.1:c.307+11212G>A	XP_011536529.1:n.307+11212G>A
XM_011538228.1:c.262+11212G>A	XP_011536530.1:n.262+11212G>A
XM_011538229.1:c.1171+11212G>A	XP_011536531.1:n.1171+11212G>A
XR_944522.1:n.2005+11212G>A
XM_011538224.3:c.1171+11212G>A	XP_011536526.1:n.1171+11212G>A
XM_011538225.3:c.808+11212G>A	XP_011536527.1:n.808+11212G>A
XM_011538226.3:c.1171+11212G>A	XP_011536528.1:n.1171+11212G>A
XM_011538229.3:c.1171+11212G>A	XP_011536531.1:n.1171+11212G>A
XM_017019208.2:c.1171+11212G>A	XP_016874697.1:n.1171+11212G>A
XM_017019209.2:c.1171+11212G>A	XP_016874698.1:n.1171+11212G>A
NM_173598.6:c.1171+11212G>A MANE Select	NP_775869.4:n.1171+11212G>A