Canonical Allele Identifier: CA384148277
Gene: KRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.25362731A>G (hg19) chr12:g.25209797A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209797A>G , CM000674.2:g.25209797A>G GRCh38
NC_000012.11:g.25362731A>G , CM000674.1:g.25362731A>G GRCh37
NC_000012.10:g.25253998A>G NCBI36
NG_007524.1:g.46124T>C
NG_007524.2:g.46207T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.226T>C ENSP00000452512.1:p.Ter76Gln
ENST00000685328.1:c.565T>C ENSP00000508921.1:p.Ter189Gln
ENST00000686877.1:c.*536T>C ENSP00000510431.1:n.*536T>C
ENST00000687356.1:c.*263T>C ENSP00000510511.1:n.*263T>C
ENST00000688228.1:n.1039T>C
ENST00000688940.1:c.565T>C ENSP00000509238.1:p.Ter189Gln
ENST00000690406.1:c.368T>C
ENST00000690804.1:c.*526T>C ENSP00000508568.1:n.*526T>C
ENST00000692768.1:c.367T>C ENSP00000510254.1:p.Ter123Gln
ENST00000693229.1:c.490T>C ENSP00000509223.1:p.Ter164Gln
ENST00000256078.10:c.*119T>C MANE Plus Clinical ENSP00000256078.5:n.*119T>C
ENST00000311936.8:c.565T>C MANE Select ENSP00000308495.3:p.Ter189Gln
ENST00000256078.8:c.*119T>C ENSP00000256078.4:n.*119T>C
ENST00000311936.7:c.565T>C ENSP00000308495.3:p.Ter189Gln
ENST00000557334.5:c.226T>C ENSP00000452512.1:p.Ter76Gln
NM_004985.4:c.565T>C NP_004976.2:p.Ter189Gln
NM_033360.3:c.*119T>C NP_203524.1:n.*119T>C
XM_011520653.1:c.565T>C XP_011518955.1:p.Ter189Gln
XM_011520653.3:c.565T>C XP_011518955.1:p.Ter189Gln
NM_001369786.1:c.*119T>C NP_001356715.1:n.*119T>C
NM_001369787.1:c.565T>C NP_001356716.1:p.Ter189Gln
NM_004985.5:c.565T>C MANE Select NP_004976.2:p.Ter189Gln
NM_033360.4:c.*119T>C MANE Plus Clinical NP_203524.1:n.*119T>C
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