Canonical Allele Identifier: CA2066114194

Gene: KSR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117522762A= , CM000674.2:g.117522762A=	GRCh38
NC_000012.11:g.117960567A= , CM000674.1:g.117960567A=	GRCh37
NC_000012.10:g.116444950A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.2219+2090T= MANE Select	ENSP00000339952.4:n.2219+2090T=
ENST00000339824.6:c.2219+2090T=	ENSP00000339952.4:n.2219+2090T=
ENST00000425217.5:c.2132+2090T=	ENSP00000389715.1:n.2132+2090T=
ENST00000545002.1:n.1365+2090T=
NM_173598.4:c.2132+2090T=	NP_775869.3:n.2132+2090T=
XM_011538224.1:c.2213+2090T=	XP_011536526.1:n.2213+2090T=
XM_011538225.1:c.1856+2090T=	XP_011536527.1:n.1856+2090T=
XM_011538226.1:c.2219+2090T=	XP_011536528.1:n.2219+2090T=
XM_011538227.1:c.1355+2090T=	XP_011536529.1:n.1355+2090T=
XM_011538228.1:c.1310+2090T=	XP_011536530.1:n.1310+2090T=
XM_011538230.1:c.959+2090T=	XP_011536532.1:n.959+2090T=
XR_944522.1:n.3053+2090T=
XM_011538224.3:c.2213+2090T=	XP_011536526.1:n.2213+2090T=
XM_011538225.3:c.1856+2090T=	XP_011536527.1:n.1856+2090T=
XM_011538226.3:c.2219+2090T=	XP_011536528.1:n.2219+2090T=
XM_017019208.2:c.2219+2090T=	XP_016874697.1:n.2219+2090T=
XM_017019210.2:c.914+2090T=	XP_016874699.1:n.914+2090T=
NM_173598.6:c.2219+2090T= MANE Select	NP_775869.4:n.2219+2090T=