Canonical Allele Identifier: CA2022884326

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209610T= , CM000674.2:g.25209610T=	GRCh38
NC_000012.11:g.25362544T= , CM000674.1:g.25362544T=	GRCh37
NC_000012.10:g.25253811T=	NCBI36
NG_007524.1:g.46311A=
NG_007524.2:g.46394A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*185A= (KRAS)	ENSP00000452512.1:n.*185A=
ENST00000685328.1:c.*185A= (KRAS)	ENSP00000508921.1:n.*185A=
ENST00000686877.1:c.*723A= (KRAS)	ENSP00000510431.1:n.*723A=
ENST00000687356.1:c.*450A= (KRAS)	ENSP00000510511.1:n.*450A=
ENST00000688940.1:c.*185A= (KRAS)	ENSP00000509238.1:n.*185A=
ENST00000690406.1:c.555A= (KRAS)
ENST00000690804.1:c.*713A= (KRAS)	ENSP00000508568.1:n.*713A=
ENST00000692768.1:c.*185A= (KRAS)	ENSP00000510254.1:n.*185A=
ENST00000693229.1:c.*185A= (KRAS)	ENSP00000509223.1:n.*185A=
ENST00000256078.10:c.*306A= (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*306A=
ENST00000311936.8:c.*185A= (KRAS) MANE Select	ENSP00000308495.3:n.*185A=
ENST00000553788.6:c.*347T= (ETFRF1)	ENSP00000451938.2:n.*347T=
ENST00000256078.8:c.*306A= (KRAS)	ENSP00000256078.4:n.*306A=
ENST00000311936.7:c.*185A= (KRAS)	ENSP00000308495.3:n.*185A=
ENST00000553788.5:c.*347T= (ETFRF1)	ENSP00000451938.1:n.*347T=
ENST00000557334.5:c.*185A= (KRAS)	ENSP00000452512.1:n.*185A=
NM_004985.4:c.*185A= (KRAS)	NP_004976.2:n.*185A=
NM_033360.3:c.*306A= (KRAS)	NP_203524.1:n.*306A=
XM_011520653.1:c.*185A= (KRAS)	XP_011518955.1:n.*185A=
XM_011520653.3:c.*185A= (KRAS)	XP_011518955.1:n.*185A=
NM_001369786.1:c.*306A= (KRAS)	NP_001356715.1:n.*306A=
NM_001369787.1:c.*185A= (KRAS)	NP_001356716.1:n.*185A=
NM_004985.5:c.*185A= (KRAS) MANE Select	NP_004976.2:n.*185A=
NM_033360.4:c.*306A= (KRAS) MANE Plus Clinical	NP_203524.1:n.*306A=