Canonical Allele Identifier: CA684170847

Gene: KSR2

Linked Data

• dbSNP Id: rs4767631
• MyVariant Identifiers: chr12:g.118311743G>C (hg19) ; chr12:g.117873938G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.117873938G>C , CM000674.2:g.117873938G>C	GRCh38
NC_000012.11:g.118311743G>C , CM000674.1:g.118311743G>C	GRCh37
NC_000012.10:g.116796126G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000339824.7:c.181-13507C>G MANE Select	ENSP00000339952.4:n.181-13507C>G
ENST00000339824.6:c.181-13507C>G	ENSP00000339952.4:n.181-13507C>G
ENST00000425217.5:c.94-13507C>G	ENSP00000389715.1:n.94-13507C>G
NM_173598.4:c.94-13507C>G	NP_775869.3:n.94-13507C>G
XM_011538224.1:c.181-13507C>G	XP_011536526.1:n.181-13507C>G
XM_011538225.1:c.-184+1746C>G	XP_011536527.1:n.-184+1746C>G
XM_011538226.1:c.181-13507C>G	XP_011536528.1:n.181-13507C>G
XM_011538229.1:c.181-13507C>G	XP_011536531.1:n.181-13507C>G
XR_944522.1:n.1015-13507C>G
XM_011538224.3:c.181-13507C>G	XP_011536526.1:n.181-13507C>G
XM_011538225.3:c.-184+1746C>G	XP_011536527.1:n.-184+1746C>G
XM_011538226.3:c.181-13507C>G	XP_011536528.1:n.181-13507C>G
XM_011538229.3:c.181-13507C>G	XP_011536531.1:n.181-13507C>G
XM_017019208.2:c.181-13507C>G	XP_016874697.1:n.181-13507C>G
XM_017019209.2:c.181-13507C>G	XP_016874698.1:n.181-13507C>G
NM_173598.6:c.181-13507C>G MANE Select	NP_775869.4:n.181-13507C>G