Canonical Allele Identifier: CA135582
Gene: KRAS HGNC NCBI
ClinGen Evidence Repository:
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209843A>G , CM000674.2:g.25209843A>G GRCh38
NC_000012.11:g.25362777A>G , CM000674.1:g.25362777A>G GRCh37
NC_000012.10:g.25254044A>G NCBI36
NG_007524.1:g.46078T>C
NG_007524.2:g.46161T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000557334.6:c.180T>C ENSP00000452512.1:p.Asp60=
ENST00000685328.1:c.519T>C ENSP00000508921.1:p.Asp173=
ENST00000686877.1:c.*490T>C ENSP00000510431.1:n.*490T>C
ENST00000687356.1:c.*217T>C ENSP00000510511.1:n.*217T>C
ENST00000688228.1:n.993T>C
ENST00000688940.1:c.519T>C ENSP00000509238.1:p.Asp173=
ENST00000690406.1:c.322T>C
ENST00000690804.1:c.*480T>C ENSP00000508568.1:n.*480T>C
ENST00000692768.1:c.321T>C ENSP00000510254.1:p.Asp107=
ENST00000693229.1:c.444T>C ENSP00000509223.1:p.Asp148=
ENST00000256078.10:c.*73T>C MANE Plus Clinical ENSP00000256078.5:n.*73T>C
ENST00000311936.8:c.519T>C MANE Select ENSP00000308495.3:p.Asp173=
ENST00000256078.8:c.*73T>C ENSP00000256078.4:n.*73T>C
ENST00000311936.7:c.519T>C ENSP00000308495.3:p.Asp173=
ENST00000557334.5:c.180T>C ENSP00000452512.1:p.Asp60=
NM_004985.4:c.519T>C NP_004976.2:p.Asp173=
NM_033360.3:c.*73T>C NP_203524.1:n.*73T>C
XM_006719069.2:c.*73T>C XP_006719132.1:n.*73T>C
XM_011520653.1:c.519T>C XP_011518955.1:p.Asp173=
XM_006719069.4:c.*73T>C XP_006719132.1:n.*73T>C
XM_011520653.3:c.519T>C XP_011518955.1:p.Asp173=
NM_001369786.1:c.*73T>C NP_001356715.1:n.*73T>C
NM_001369787.1:c.519T>C NP_001356716.1:p.Asp173=
NM_004985.5:c.519T>C MANE Select NP_004976.2:p.Asp173=
NM_033360.4:c.*73T>C MANE Plus Clinical NP_203524.1:n.*73T>C