Canonical Allele Identifier: CA2022884511

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209804_25209806delinsTAC , CM000674.2:g.25209804_25209806delinsTAC	GRCh38
NC_000012.11:g.25362738_25362740delinsTAC , CM000674.1:g.25362738_25362740delinsTAC	GRCh37
NC_000012.10:g.25254005_25254007delinsTAC	NCBI36
NG_007524.1:g.46115_46117delinsGTA
NG_007524.2:g.46198_46200delinsGTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.217_219delinsGTA	ENSP00000452512.1:p.Val73=
ENST00000685328.1:c.556_558delinsGTA	ENSP00000508921.1:p.Val186=
ENST00000686877.1:c.*527_*529delinsGTA	ENSP00000510431.1:n.*527_*529delinsGTA
ENST00000687356.1:c.*254_*256delinsGTA	ENSP00000510511.1:n.*254_*256delinsGTA
ENST00000688228.1:n.1030_1032delinsGTA
ENST00000688940.1:c.556_558delinsGTA	ENSP00000509238.1:p.Val186=
ENST00000690406.1:c.359_361delinsGTA
ENST00000690804.1:c.*517_*519delinsGTA	ENSP00000508568.1:n.*517_*519delinsGTA
ENST00000692768.1:c.358_360delinsGTA	ENSP00000510254.1:p.Val120=
ENST00000693229.1:c.481_483delinsGTA	ENSP00000509223.1:p.Val161=
ENST00000256078.10:c.*110_*112delinsGTA MANE Plus Clinical	ENSP00000256078.5:n.*110_*112delinsGTA
ENST00000311936.8:c.556_558delinsGTA MANE Select	ENSP00000308495.3:p.Val186=
ENST00000256078.8:c.*110_*112delinsGTA	ENSP00000256078.4:n.*110_*112delinsGTA
ENST00000311936.7:c.556_558delinsGTA	ENSP00000308495.3:p.Val186=
ENST00000557334.5:c.217_219delinsGTA	ENSP00000452512.1:p.Val73=
NM_004985.4:c.556_558delinsGTA	NP_004976.2:p.Val186=
NM_033360.3:c.*110_*112delinsGTA	NP_203524.1:n.*110_*112delinsGTA
XM_011520653.1:c.556_558delinsGTA	XP_011518955.1:p.Val186=
XM_011520653.3:c.556_558delinsGTA	XP_011518955.1:p.Val186=
NM_001369786.1:c.*110_*112delinsGTA	NP_001356715.1:n.*110_*112delinsGTA
NM_001369787.1:c.556_558delinsGTA	NP_001356716.1:p.Val186=
NM_004985.5:c.556_558delinsGTA MANE Select	NP_004976.2:p.Val186=
NM_033360.4:c.*110_*112delinsGTA MANE Plus Clinical	NP_203524.1:n.*110_*112delinsGTA