Canonical Allele Identifier: CA2022884368

Gene: KRAS ETFRF1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209640G= , CM000674.2:g.25209640G=	GRCh38
NC_000012.11:g.25362574G= , CM000674.1:g.25362574G=	GRCh37
NC_000012.10:g.25253841G=	NCBI36
NG_007524.1:g.46281C=
NG_007524.2:g.46364C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*155C= (KRAS)	ENSP00000452512.1:n.*155C=
ENST00000685328.1:c.*155C= (KRAS)	ENSP00000508921.1:n.*155C=
ENST00000686877.1:c.*693C= (KRAS)	ENSP00000510431.1:n.*693C=
ENST00000687356.1:c.*420C= (KRAS)	ENSP00000510511.1:n.*420C=
ENST00000688940.1:c.*155C= (KRAS)	ENSP00000509238.1:n.*155C=
ENST00000690406.1:c.525C= (KRAS)
ENST00000690804.1:c.*683C= (KRAS)	ENSP00000508568.1:n.*683C=
ENST00000692768.1:c.*155C= (KRAS)	ENSP00000510254.1:n.*155C=
ENST00000693229.1:c.*155C= (KRAS)	ENSP00000509223.1:n.*155C=
ENST00000256078.10:c.*276C= (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*276C=
ENST00000311936.8:c.*155C= (KRAS) MANE Select	ENSP00000308495.3:n.*155C=
ENST00000553788.6:c.*377G= (ETFRF1)	ENSP00000451938.2:n.*377G=
ENST00000256078.8:c.*276C= (KRAS)	ENSP00000256078.4:n.*276C=
ENST00000311936.7:c.*155C= (KRAS)	ENSP00000308495.3:n.*155C=
ENST00000553788.5:c.*377G= (ETFRF1)	ENSP00000451938.1:n.*377G=
ENST00000557334.5:c.*155C= (KRAS)	ENSP00000452512.1:n.*155C=
NM_004985.4:c.*155C= (KRAS)	NP_004976.2:n.*155C=
NM_033360.3:c.*276C= (KRAS)	NP_203524.1:n.*276C=
XM_011520653.1:c.*155C= (KRAS)	XP_011518955.1:n.*155C=
XM_011520653.3:c.*155C= (KRAS)	XP_011518955.1:n.*155C=
NM_001369786.1:c.*276C= (KRAS)	NP_001356715.1:n.*276C=
NM_001369787.1:c.*155C= (KRAS)	NP_001356716.1:n.*155C=
NM_004985.5:c.*155C= (KRAS) MANE Select	NP_004976.2:n.*155C=
NM_033360.4:c.*276C= (KRAS) MANE Plus Clinical	NP_203524.1:n.*276C=