Canonical Allele Identifier: CA2066285552

Gene: KSR2

Linked Data

• dbSNP Id: rs1895166880

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117916149_117916150insC , CM000674.2:g.117916149_117916150insC	GRCh38
NC_000012.11:g.118353954_118353955insC , CM000674.1:g.118353954_118353955insC	GRCh37
NC_000012.10:g.116838337_116838338insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.180+51926_180+51927insG MANE Select	ENSP00000339952.4:n.180+51926_180+51927insG
ENST00000339824.6:c.180+51926_180+51927insG	ENSP00000339952.4:n.180+51926_180+51927insG
ENST00000425217.5:c.93+51926_93+51927insG	ENSP00000389715.1:n.93+51926_93+51927insG
NM_173598.4:c.93+51926_93+51927insG	NP_775869.3:n.93+51926_93+51927insG
XM_011538224.1:c.180+51926_180+51927insG	XP_011536526.1:n.180+51926_180+51927insG
XM_011538226.1:c.180+51926_180+51927insG	XP_011536528.1:n.180+51926_180+51927insG
XM_011538229.1:c.180+51926_180+51927insG	XP_011536531.1:n.180+51926_180+51927insG
XR_944522.1:n.1014+51926_1014+51927insG
XM_011538224.3:c.180+51926_180+51927insG	XP_011536526.1:n.180+51926_180+51927insG
XM_011538226.3:c.180+51926_180+51927insG	XP_011536528.1:n.180+51926_180+51927insG
XM_011538229.3:c.180+51926_180+51927insG	XP_011536531.1:n.180+51926_180+51927insG
XM_017019208.2:c.180+51926_180+51927insG	XP_016874697.1:n.180+51926_180+51927insG
XM_017019209.2:c.180+51926_180+51927insG	XP_016874698.1:n.180+51926_180+51927insG
NM_173598.6:c.180+51926_180+51927insG MANE Select	NP_775869.4:n.180+51926_180+51927insG