Canonical Allele Identifier: CA2022880785

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206041T= , CM000674.2:g.25206041T=	GRCh38
NC_000012.11:g.25358975T= , CM000674.1:g.25358975T=	GRCh37
NC_000012.10:g.25250242T=	NCBI36
NG_007524.1:g.49880A=
NG_007524.2:g.49963A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000685328.1:c.*3754A= (KRAS)	ENSP00000508921.1:n.*3754A=
ENST00000686877.1:c.*4292A= (KRAS)	ENSP00000510431.1:n.*4292A=
ENST00000687356.1:c.*4019A= (KRAS)	ENSP00000510511.1:n.*4019A=
ENST00000690406.1:c.4124A= (KRAS)
ENST00000692768.1:c.*3754A= (KRAS)	ENSP00000510254.1:n.*3754A=
ENST00000693229.1:c.*3754A= (KRAS)	ENSP00000509223.1:n.*3754A=
ENST00000256078.10:c.*3875A= (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3875A=
ENST00000311936.8:c.*3754A= (KRAS) MANE Select	ENSP00000308495.3:n.*3754A=
ENST00000553788.6:c.51+2034T= (ETFRF1)	ENSP00000451938.2:n.51+2034T=
ENST00000311936.7:c.*3754A= (KRAS)	ENSP00000308495.3:n.*3754A=
ENST00000553788.5:c.45+2034T= (ETFRF1)	ENSP00000451938.1:n.45+2034T=
NM_004985.4:c.*3754A= (KRAS)	NP_004976.2:n.*3754A=
NM_033360.3:c.*3875A= (KRAS)	NP_203524.1:n.*3875A=
XM_011520653.1:c.*3754A= (KRAS)	XP_011518955.1:n.*3754A=
XM_011520653.3:c.*3754A= (KRAS)	XP_011518955.1:n.*3754A=
NM_001369786.1:c.*3875A= (KRAS)	NP_001356715.1:n.*3875A=
NM_001369787.1:c.*3754A= (KRAS)	NP_001356716.1:n.*3754A=
NM_004985.5:c.*3754A= (KRAS) MANE Select	NP_004976.2:n.*3754A=
NM_033360.4:c.*3875A= (KRAS) MANE Plus Clinical	NP_203524.1:n.*3875A=