Canonical Allele Identifier: CA2022882997

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208207C= , CM000674.2:g.25208207C=	GRCh38
NC_000012.11:g.25361141C= , CM000674.1:g.25361141C=	GRCh37
NC_000012.10:g.25252408C=	NCBI36
NG_007524.1:g.47714G=
NG_007524.2:g.47797G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1588G= (KRAS)	ENSP00000508921.1:n.*1588G=
ENST00000686877.1:c.*2126G= (KRAS)	ENSP00000510431.1:n.*2126G=
ENST00000687356.1:c.*1853G= (KRAS)	ENSP00000510511.1:n.*1853G=
ENST00000688940.1:c.*1588G= (KRAS)	ENSP00000509238.1:n.*1588G=
ENST00000690406.1:c.1958G= (KRAS)
ENST00000690804.1:c.*2116G= (KRAS)	ENSP00000508568.1:n.*2116G=
ENST00000692768.1:c.*1588G= (KRAS)	ENSP00000510254.1:n.*1588G=
ENST00000693229.1:c.*1588G= (KRAS)	ENSP00000509223.1:n.*1588G=
ENST00000256078.10:c.*1709G= (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1709G=
ENST00000311936.8:c.*1588G= (KRAS) MANE Select	ENSP00000308495.3:n.*1588G=
ENST00000553788.6:c.52-988C= (ETFRF1)	ENSP00000451938.2:n.52-988C=
ENST00000311936.7:c.*1588G= (KRAS)	ENSP00000308495.3:n.*1588G=
ENST00000553788.5:c.46-988C= (ETFRF1)	ENSP00000451938.1:n.46-988C=
NM_004985.4:c.*1588G= (KRAS)	NP_004976.2:n.*1588G=
NM_033360.3:c.*1709G= (KRAS)	NP_203524.1:n.*1709G=
XM_011520653.1:c.*1588G= (KRAS)	XP_011518955.1:n.*1588G=
XM_011520653.3:c.*1588G= (KRAS)	XP_011518955.1:n.*1588G=
NM_001369786.1:c.*1709G= (KRAS)	NP_001356715.1:n.*1709G=
NM_001369787.1:c.*1588G= (KRAS)	NP_001356716.1:n.*1588G=
NM_004985.5:c.*1588G= (KRAS) MANE Select	NP_004976.2:n.*1588G=
NM_033360.4:c.*1709G= (KRAS) MANE Plus Clinical	NP_203524.1:n.*1709G=