Canonical Allele Identifier: CA245067519

Gene: KSR2

Linked Data

• dbSNP Id: rs1025325716
• gnomAD v3: 12-117668298-C-G
• gnomAD v4: 12-117668298-C-G
• MyVariant Identifiers: chr12:g.118106103C>G (hg19) ; chr12:g.117668298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117668298C>G , CM000674.2:g.117668298C>G	GRCh38
NC_000012.11:g.118106103C>G , CM000674.1:g.118106103C>G	GRCh37
NC_000012.10:g.116590486C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339824.7:c.987-640G>C MANE Select	ENSP00000339952.4:n.987-640G>C
ENST00000339824.6:c.987-640G>C	ENSP00000339952.4:n.987-640G>C
ENST00000425217.5:c.900-640G>C	ENSP00000389715.1:n.900-640G>C
ENST00000545002.1:n.133-640G>C
NM_173598.4:c.900-640G>C	NP_775869.3:n.900-640G>C
XM_011538224.1:c.987-640G>C	XP_011536526.1:n.987-640G>C
XM_011538225.1:c.624-640G>C	XP_011536527.1:n.624-640G>C
XM_011538226.1:c.987-640G>C	XP_011536528.1:n.987-640G>C
XM_011538227.1:c.123-640G>C	XP_011536529.1:n.123-640G>C
XM_011538228.1:c.78-640G>C	XP_011536530.1:n.78-640G>C
XM_011538229.1:c.987-640G>C	XP_011536531.1:n.987-640G>C
XR_944522.1:n.1821-640G>C
XM_011538224.3:c.987-640G>C	XP_011536526.1:n.987-640G>C
XM_011538225.3:c.624-640G>C	XP_011536527.1:n.624-640G>C
XM_011538226.3:c.987-640G>C	XP_011536528.1:n.987-640G>C
XM_011538229.3:c.987-640G>C	XP_011536531.1:n.987-640G>C
XM_017019208.2:c.987-640G>C	XP_016874697.1:n.987-640G>C
XM_017019209.2:c.987-640G>C	XP_016874698.1:n.987-640G>C
NM_173598.6:c.987-640G>C MANE Select	NP_775869.4:n.987-640G>C