Canonical Allele Identifier: CA384149261

Gene: KRAS

Linked Data

• ClinVar Variation Id: 2581679
• ClinVar RCV Id: RCV003330455
• dbSNP Id: rs989151052
• MyVariant Identifiers: chr12:g.25368484T>A (hg19) ; chr12:g.25215550T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215550T>A , CM000674.2:g.25215550T>A	GRCh38
NC_000012.11:g.25368484T>A , CM000674.1:g.25368484T>A	GRCh37
NC_000012.10:g.25259751T>A	NCBI36
NG_007524.1:g.40371A>T
NG_007524.2:g.40454A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-5639A>T	ENSP00000452512.1:n.112-5639A>T
ENST00000685328.1:c.451-5639A>T	ENSP00000508921.1:n.451-5639A>T
ENST00000686877.1:c.*422-5639A>T	ENSP00000510431.1:n.*422-5639A>T
ENST00000687356.1:c.*149-5639A>T	ENSP00000510511.1:n.*149-5639A>T
ENST00000688228.1:n.925-5639A>T
ENST00000688940.1:c.451-5639A>T	ENSP00000509238.1:n.451-5639A>T
ENST00000690406.1:c.161-2344A>T
ENST00000690804.1:c.*412-5639A>T	ENSP00000508568.1:n.*412-5639A>T
ENST00000692768.1:c.253-5639A>T	ENSP00000510254.1:n.253-5639A>T
ENST00000693229.1:c.376-5639A>T	ENSP00000509223.1:n.376-5639A>T
ENST00000256078.10:c.461A>T MANE Plus Clinical	ENSP00000256078.5:p.Asp154Val
ENST00000311936.8:c.451-5639A>T MANE Select	ENSP00000308495.3:n.451-5639A>T
ENST00000256078.8:c.461A>T	ENSP00000256078.4:p.Asp154Val
ENST00000311936.7:c.451-5639A>T	ENSP00000308495.3:n.451-5639A>T
ENST00000557334.5:c.112-5639A>T	ENSP00000452512.1:n.112-5639A>T
NM_004985.4:c.451-5639A>T	NP_004976.2:n.451-5639A>T
NM_033360.3:c.461A>T	NP_203524.1:p.Asp154Val
XM_006719069.2:c.461A>T	XP_006719132.1:p.Asp154Val
XM_011520653.1:c.451-5639A>T	XP_011518955.1:n.451-5639A>T
XM_006719069.4:c.461A>T	XP_006719132.1:p.Asp154Val
XM_011520653.3:c.451-5639A>T	XP_011518955.1:n.451-5639A>T
NM_001369786.1:c.461A>T	NP_001356715.1:p.Asp154Val
NM_001369787.1:c.451-5639A>T	NP_001356716.1:n.451-5639A>T
NM_004985.5:c.451-5639A>T MANE Select	NP_004976.2:n.451-5639A>T
NM_033360.4:c.461A>T MANE Plus Clinical	NP_203524.1:p.Asp154Val