Canonical Allele Identifier: CA2066089252

Gene: KSR2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117500714C>G , CM000674.2:g.117500714C>G	GRCh38
NC_000012.11:g.117938519C>G , CM000674.1:g.117938519C>G	GRCh37
NC_000012.10:g.116422902C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339824.7:c.2220-15023G>C MANE Select	ENSP00000339952.4:n.2220-15023G>C
ENST00000339824.6:c.2220-15023G>C	ENSP00000339952.4:n.2220-15023G>C
ENST00000425217.5:c.2133-15023G>C	ENSP00000389715.1:n.2133-15023G>C
NM_173598.4:c.2133-15023G>C	NP_775869.3:n.2133-15023G>C
XM_011538224.1:c.2214-15023G>C	XP_011536526.1:n.2214-15023G>C
XM_011538225.1:c.1857-15023G>C	XP_011536527.1:n.1857-15023G>C
XM_011538227.1:c.1356-15023G>C	XP_011536529.1:n.1356-15023G>C
XM_011538228.1:c.1311-15023G>C	XP_011536530.1:n.1311-15023G>C
XM_011538230.1:c.960-15023G>C	XP_011536532.1:n.960-15023G>C
XR_944522.1:n.3054-15023G>C
XM_011538224.3:c.2214-15023G>C	XP_011536526.1:n.2214-15023G>C
XM_011538225.3:c.1857-15023G>C	XP_011536527.1:n.1857-15023G>C
XM_017019208.2:c.2220-15023G>C	XP_016874697.1:n.2220-15023G>C
XM_017019210.2:c.915-15023G>C	XP_016874699.1:n.915-15023G>C
NM_173598.6:c.2220-15023G>C MANE Select	NP_775869.4:n.2220-15023G>C