Canonical Allele Identifier: CA2022883048

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208244A= , CM000674.2:g.25208244A=	GRCh38
NC_000012.11:g.25361178A= , CM000674.1:g.25361178A=	GRCh37
NC_000012.10:g.25252445A=	NCBI36
NG_007524.1:g.47677T=
NG_007524.2:g.47760T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1551T= (KRAS)	ENSP00000508921.1:n.*1551T=
ENST00000686877.1:c.*2089T= (KRAS)	ENSP00000510431.1:n.*2089T=
ENST00000687356.1:c.*1816T= (KRAS)	ENSP00000510511.1:n.*1816T=
ENST00000688940.1:c.*1551T= (KRAS)	ENSP00000509238.1:n.*1551T=
ENST00000690406.1:c.1921T= (KRAS)
ENST00000690804.1:c.*2079T= (KRAS)	ENSP00000508568.1:n.*2079T=
ENST00000692768.1:c.*1551T= (KRAS)	ENSP00000510254.1:n.*1551T=
ENST00000693229.1:c.*1551T= (KRAS)	ENSP00000509223.1:n.*1551T=
ENST00000256078.10:c.*1672T= (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1672T=
ENST00000311936.8:c.*1551T= (KRAS) MANE Select	ENSP00000308495.3:n.*1551T=
ENST00000553788.6:c.52-951A= (ETFRF1)	ENSP00000451938.2:n.52-951A=
ENST00000311936.7:c.*1551T= (KRAS)	ENSP00000308495.3:n.*1551T=
ENST00000553788.5:c.46-951A= (ETFRF1)	ENSP00000451938.1:n.46-951A=
NM_004985.4:c.*1551T= (KRAS)	NP_004976.2:n.*1551T=
NM_033360.3:c.*1672T= (KRAS)	NP_203524.1:n.*1672T=
XM_011520653.1:c.*1551T= (KRAS)	XP_011518955.1:n.*1551T=
XM_011520653.3:c.*1551T= (KRAS)	XP_011518955.1:n.*1551T=
NM_001369786.1:c.*1672T= (KRAS)	NP_001356715.1:n.*1672T=
NM_001369787.1:c.*1551T= (KRAS)	NP_001356716.1:n.*1551T=
NM_004985.5:c.*1551T= (KRAS) MANE Select	NP_004976.2:n.*1551T=
NM_033360.4:c.*1672T= (KRAS) MANE Plus Clinical	NP_203524.1:n.*1672T=