Canonical Allele Identifier: CA10632488

Linked Data

ClinVar Variation Id: 308114
ClinVar RCV Id: RCV000388634
dbSNP Id: rs61763589

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25208971A>G , CM000674.2:g.25208971A>G GRCh38
NC_000012.11:g.25361905A>G , CM000674.1:g.25361905A>G GRCh37
NC_000012.10:g.25253172A>G NCBI36
NG_007524.1:g.46950T>C
NG_007524.2:g.47033T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*824T>C (KRAS) ENSP00000508921.1:n.*824T>C
ENST00000686877.1:c.*1362T>C (KRAS) ENSP00000510431.1:n.*1362T>C
ENST00000687356.1:c.*1089T>C (KRAS) ENSP00000510511.1:n.*1089T>C
ENST00000688940.1:c.*824T>C (KRAS) ENSP00000509238.1:n.*824T>C
ENST00000690406.1:c.1194T>C (KRAS)
ENST00000690804.1:c.*1352T>C (KRAS) ENSP00000508568.1:n.*1352T>C
ENST00000692768.1:c.*824T>C (KRAS) ENSP00000510254.1:n.*824T>C
ENST00000693229.1:c.*824T>C (KRAS) ENSP00000509223.1:n.*824T>C
ENST00000256078.10:c.*945T>C (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*945T>C
ENST00000311936.8:c.*824T>C (KRAS) MANE Select ENSP00000308495.3:n.*824T>C
ENST00000553788.6:c.52-224A>G (ETFRF1) ENSP00000451938.2:n.52-224A>G
ENST00000311936.7:c.*824T>C (KRAS) ENSP00000308495.3:n.*824T>C
ENST00000553788.5:c.46-224A>G (ETFRF1) ENSP00000451938.1:n.46-224A>G
NM_004985.4:c.*824T>C (KRAS) NP_004976.2:n.*824T>C
NM_033360.3:c.*945T>C (KRAS) NP_203524.1:n.*945T>C
XM_011520653.1:c.*824T>C (KRAS) XP_011518955.1:n.*824T>C
XM_011520653.3:c.*824T>C (KRAS) XP_011518955.1:n.*824T>C
NM_001369786.1:c.*945T>C (KRAS) NP_001356715.1:n.*945T>C
NM_001369787.1:c.*824T>C (KRAS) NP_001356716.1:n.*824T>C
NM_004985.5:c.*824T>C (KRAS) MANE Select NP_004976.2:n.*824T>C
NM_033360.4:c.*945T>C (KRAS) MANE Plus Clinical NP_203524.1:n.*945T>C