Canonical Allele Identifier: CA2022906614

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225831C= , CM000674.2:g.25225831C=	GRCh38
NC_000012.11:g.25378765C= , CM000674.1:g.25378765C=	GRCh37
NC_000012.10:g.25270032C=	NCBI36
NG_007524.1:g.30090G=
NG_007524.2:g.30173G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15920G=	ENSP00000452512.1:n.112-15920G=
ENST00000685328.1:c.291-58G=	ENSP00000508921.1:n.291-58G=
ENST00000686877.1:c.*262-58G=	ENSP00000510431.1:n.*262-58G=
ENST00000687356.1:c.112-58G=	ENSP00000510511.1:n.112-58G=
ENST00000688228.1:n.765-58G=
ENST00000688940.1:c.291-58G=	ENSP00000509238.1:n.291-58G=
ENST00000690804.1:c.*252-58G=	ENSP00000508568.1:n.*252-58G=
ENST00000692768.1:c.93-58G=	ENSP00000510254.1:n.93-58G=
ENST00000693229.1:c.216-58G=	ENSP00000509223.1:n.216-58G=
ENST00000256078.10:c.291-58G= MANE Plus Clinical	ENSP00000256078.5:n.291-58G=
ENST00000311936.8:c.291-58G= MANE Select	ENSP00000308495.3:n.291-58G=
ENST00000256078.8:c.291-58G=	ENSP00000256078.4:n.291-58G=
ENST00000311936.7:c.291-58G=	ENSP00000308495.3:n.291-58G=
ENST00000557334.5:c.112-15920G=	ENSP00000452512.1:n.112-15920G=
NM_004985.4:c.291-58G=	NP_004976.2:n.291-58G=
NM_033360.3:c.291-58G=	NP_203524.1:n.291-58G=
XM_006719069.2:c.291-58G=	XP_006719132.1:n.291-58G=
XM_011520653.1:c.291-58G=	XP_011518955.1:n.291-58G=
XM_006719069.4:c.291-58G=	XP_006719132.1:n.291-58G=
XM_011520653.3:c.291-58G=	XP_011518955.1:n.291-58G=
NM_001369786.1:c.291-58G=	NP_001356715.1:n.291-58G=
NM_001369787.1:c.291-58G=	NP_001356716.1:n.291-58G=
NM_004985.5:c.291-58G= MANE Select	NP_004976.2:n.291-58G=
NM_033360.4:c.291-58G= MANE Plus Clinical	NP_203524.1:n.291-58G=