Canonical Allele Identifier: CA2794888710

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209712A>C , CM000674.2:g.25209712A>C	GRCh38
NC_000012.11:g.25362646A>C , CM000674.1:g.25362646A>C	GRCh37
NC_000012.10:g.25253913A>C	NCBI36
NG_007524.1:g.46209T>G
NG_007524.2:g.46292T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*83T>G	ENSP00000452512.1:n.*83T>G
ENST00000685328.1:c.*83T>G	ENSP00000508921.1:n.*83T>G
ENST00000686877.1:c.*621T>G	ENSP00000510431.1:n.*621T>G
ENST00000687356.1:c.*348T>G	ENSP00000510511.1:n.*348T>G
ENST00000688228.1:n.1124T>G
ENST00000688940.1:c.*83T>G	ENSP00000509238.1:n.*83T>G
ENST00000690406.1:c.453T>G
ENST00000690804.1:c.*611T>G	ENSP00000508568.1:n.*611T>G
ENST00000692768.1:c.*83T>G	ENSP00000510254.1:n.*83T>G
ENST00000693229.1:c.*83T>G	ENSP00000509223.1:n.*83T>G
ENST00000256078.10:c.*204T>G MANE Plus Clinical	ENSP00000256078.5:n.*204T>G
ENST00000311936.8:c.*83T>G MANE Select	ENSP00000308495.3:n.*83T>G
ENST00000256078.8:c.*204T>G	ENSP00000256078.4:n.*204T>G
ENST00000311936.7:c.*83T>G	ENSP00000308495.3:n.*83T>G
ENST00000557334.5:c.*83T>G	ENSP00000452512.1:n.*83T>G
NM_004985.4:c.*83T>G	NP_004976.2:n.*83T>G
NM_033360.3:c.*204T>G	NP_203524.1:n.*204T>G
XM_011520653.1:c.*83T>G	XP_011518955.1:n.*83T>G
XM_011520653.3:c.*83T>G	XP_011518955.1:n.*83T>G
NM_001369786.1:c.*204T>G	NP_001356715.1:n.*204T>G
NM_001369787.1:c.*83T>G	NP_001356716.1:n.*83T>G
NM_004985.5:c.*83T>G MANE Select	NP_004976.2:n.*83T>G
NM_033360.4:c.*204T>G MANE Plus Clinical	NP_203524.1:n.*204T>G