Canonical Allele Identifier: CA15770430
Gene: KSR2 HGNC NCBI

Linked Data

dbSNP Id: rs1846644

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.117500575T>C , CM000674.2:g.117500575T>C GRCh38
NC_000012.11:g.117938380T>C , CM000674.1:g.117938380T>C GRCh37
NC_000012.10:g.116422763T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000339824.7:c.2220-14884A>G MANE Select ENSP00000339952.4:n.2220-14884A>G
ENST00000339824.6:c.2220-14884A>G ENSP00000339952.4:n.2220-14884A>G
ENST00000425217.5:c.2133-14884A>G ENSP00000389715.1:n.2133-14884A>G
NM_173598.4:c.2133-14884A>G NP_775869.3:n.2133-14884A>G
XM_011538224.1:c.2214-14884A>G XP_011536526.1:n.2214-14884A>G
XM_011538225.1:c.1857-14884A>G XP_011536527.1:n.1857-14884A>G
XM_011538227.1:c.1356-14884A>G XP_011536529.1:n.1356-14884A>G
XM_011538228.1:c.1311-14884A>G XP_011536530.1:n.1311-14884A>G
XM_011538230.1:c.960-14884A>G XP_011536532.1:n.960-14884A>G
XR_944522.1:n.3054-14884A>G
XM_011538224.3:c.2214-14884A>G XP_011536526.1:n.2214-14884A>G
XM_011538225.3:c.1857-14884A>G XP_011536527.1:n.1857-14884A>G
XM_017019208.2:c.2220-14884A>G XP_016874697.1:n.2220-14884A>G
XM_017019210.2:c.915-14884A>G XP_016874699.1:n.915-14884A>G
NM_173598.6:c.2220-14884A>G MANE Select NP_775869.4:n.2220-14884A>G