Canonical Allele Identifier: CA2066173118

Gene: KSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117668339_117668342delinsTACC , CM000674.2:g.117668339_117668342delinsTACC	GRCh38
NC_000012.11:g.118106144_118106147delinsTACC , CM000674.1:g.118106144_118106147delinsTACC	GRCh37
NC_000012.10:g.116590527_116590530delinsTACC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339824.7:c.987-684_987-681delinsGGTA MANE Select	ENSP00000339952.4:n.987-684_987-681delinsGGTA
ENST00000339824.6:c.987-684_987-681delinsGGTA	ENSP00000339952.4:n.987-684_987-681delinsGGTA
ENST00000425217.5:c.900-684_900-681delinsGGTA	ENSP00000389715.1:n.900-684_900-681delinsGGTA
ENST00000545002.1:n.133-684_133-681delinsGGTA
NM_173598.4:c.900-684_900-681delinsGGTA	NP_775869.3:n.900-684_900-681delinsGGTA
XM_011538224.1:c.987-684_987-681delinsGGTA	XP_011536526.1:n.987-684_987-681delinsGGTA
XM_011538225.1:c.624-684_624-681delinsGGTA	XP_011536527.1:n.624-684_624-681delinsGGTA
XM_011538226.1:c.987-684_987-681delinsGGTA	XP_011536528.1:n.987-684_987-681delinsGGTA
XM_011538227.1:c.123-684_123-681delinsGGTA	XP_011536529.1:n.123-684_123-681delinsGGTA
XM_011538228.1:c.78-684_78-681delinsGGTA	XP_011536530.1:n.78-684_78-681delinsGGTA
XM_011538229.1:c.987-684_987-681delinsGGTA	XP_011536531.1:n.987-684_987-681delinsGGTA
XR_944522.1:n.1821-684_1821-681delinsGGTA
XM_011538224.3:c.987-684_987-681delinsGGTA	XP_011536526.1:n.987-684_987-681delinsGGTA
XM_011538225.3:c.624-684_624-681delinsGGTA	XP_011536527.1:n.624-684_624-681delinsGGTA
XM_011538226.3:c.987-684_987-681delinsGGTA	XP_011536528.1:n.987-684_987-681delinsGGTA
XM_011538229.3:c.987-684_987-681delinsGGTA	XP_011536531.1:n.987-684_987-681delinsGGTA
XM_017019208.2:c.987-684_987-681delinsGGTA	XP_016874697.1:n.987-684_987-681delinsGGTA
XM_017019209.2:c.987-684_987-681delinsGGTA	XP_016874698.1:n.987-684_987-681delinsGGTA
NM_173598.6:c.987-684_987-681delinsGGTA MANE Select	NP_775869.4:n.987-684_987-681delinsGGTA