Canonical Allele Identifier: CA2066285560
Gene: KSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1895167057

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117916154_117916155insTATTTG , CM000674.2:g.117916154_117916155insTATTTG GRCh38
NC_000012.11:g.118353959_118353960insTATTTG , CM000674.1:g.118353959_118353960insTATTTG GRCh37
NC_000012.10:g.116838342_116838343insTATTTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339824.7:c.180+51921_180+51922insCAAATA MANE Select ENSP00000339952.4:n.180+51921_180+51922insCAAATA
ENST00000339824.6:c.180+51921_180+51922insCAAATA ENSP00000339952.4:n.180+51921_180+51922insCAAATA
ENST00000425217.5:c.93+51921_93+51922insCAAATA ENSP00000389715.1:n.93+51921_93+51922insCAAATA
NM_173598.4:c.93+51921_93+51922insCAAATA NP_775869.3:n.93+51921_93+51922insCAAATA
XM_011538224.1:c.180+51921_180+51922insCAAATA XP_011536526.1:n.180+51921_180+51922insCAAATA
XM_011538226.1:c.180+51921_180+51922insCAAATA XP_011536528.1:n.180+51921_180+51922insCAAATA
XM_011538229.1:c.180+51921_180+51922insCAAATA XP_011536531.1:n.180+51921_180+51922insCAAATA
XR_944522.1:n.1014+51921_1014+51922insCAAATA
XM_011538224.3:c.180+51921_180+51922insCAAATA XP_011536526.1:n.180+51921_180+51922insCAAATA
XM_011538226.3:c.180+51921_180+51922insCAAATA XP_011536528.1:n.180+51921_180+51922insCAAATA
XM_011538229.3:c.180+51921_180+51922insCAAATA XP_011536531.1:n.180+51921_180+51922insCAAATA
XM_017019208.2:c.180+51921_180+51922insCAAATA XP_016874697.1:n.180+51921_180+51922insCAAATA
XM_017019209.2:c.180+51921_180+51922insCAAATA XP_016874698.1:n.180+51921_180+51922insCAAATA
NM_173598.6:c.180+51921_180+51922insCAAATA MANE Select NP_775869.4:n.180+51921_180+51922insCAAATA