Canonical Allele Identifier: CA2066285473
Gene: KSR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117916132_117916138delinsCTTCTTT , CM000674.2:g.117916132_117916138delinsCTTCTTT GRCh38
NC_000012.11:g.118353937_118353943delinsCTTCTTT , CM000674.1:g.118353937_118353943delinsCTTCTTT GRCh37
NC_000012.10:g.116838320_116838326delinsCTTCTTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000339824.7:c.180+51938_180+51944delinsAAAGAAG MANE Select ENSP00000339952.4:n.180+51938_180+51944delinsAAAGAAG
ENST00000339824.6:c.180+51938_180+51944delinsAAAGAAG ENSP00000339952.4:n.180+51938_180+51944delinsAAAGAAG
ENST00000425217.5:c.93+51938_93+51944delinsAAAGAAG ENSP00000389715.1:n.93+51938_93+51944delinsAAAGAAG
NM_173598.4:c.93+51938_93+51944delinsAAAGAAG NP_775869.3:n.93+51938_93+51944delinsAAAGAAG
XM_011538224.1:c.180+51938_180+51944delinsAAAGAAG XP_011536526.1:n.180+51938_180+51944delinsAAAGAAG
XM_011538226.1:c.180+51938_180+51944delinsAAAGAAG XP_011536528.1:n.180+51938_180+51944delinsAAAGAAG
XM_011538229.1:c.180+51938_180+51944delinsAAAGAAG XP_011536531.1:n.180+51938_180+51944delinsAAAGAAG
XR_944522.1:n.1014+51938_1014+51944delinsAAAGAAG
XM_011538224.3:c.180+51938_180+51944delinsAAAGAAG XP_011536526.1:n.180+51938_180+51944delinsAAAGAAG
XM_011538226.3:c.180+51938_180+51944delinsAAAGAAG XP_011536528.1:n.180+51938_180+51944delinsAAAGAAG
XM_011538229.3:c.180+51938_180+51944delinsAAAGAAG XP_011536531.1:n.180+51938_180+51944delinsAAAGAAG
XM_017019208.2:c.180+51938_180+51944delinsAAAGAAG XP_016874697.1:n.180+51938_180+51944delinsAAAGAAG
XM_017019209.2:c.180+51938_180+51944delinsAAAGAAG XP_016874698.1:n.180+51938_180+51944delinsAAAGAAG
NM_173598.6:c.180+51938_180+51944delinsAAAGAAG MANE Select NP_775869.4:n.180+51938_180+51944delinsAAAGAAG