Canonical Allele Identifier: CA654638094

Gene: KRAS ETFRF1

Linked Data

• gnomAD v4: 12-25209633-T-G
• COSMIC: COSN26603031

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209633T>G , CM000674.2:g.25209633T>G	GRCh38
NC_000012.11:g.25362567T>G , CM000674.1:g.25362567T>G	GRCh37
NC_000012.10:g.25253834T>G	NCBI36
NG_007524.1:g.46288A>C
NG_007524.2:g.46371A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*162A>C (KRAS)	ENSP00000452512.1:n.*162A>C
ENST00000685328.1:c.*162A>C (KRAS)	ENSP00000508921.1:n.*162A>C
ENST00000686877.1:c.*700A>C (KRAS)	ENSP00000510431.1:n.*700A>C
ENST00000687356.1:c.*427A>C (KRAS)	ENSP00000510511.1:n.*427A>C
ENST00000688940.1:c.*162A>C (KRAS)	ENSP00000509238.1:n.*162A>C
ENST00000690406.1:c.532A>C (KRAS)
ENST00000690804.1:c.*690A>C (KRAS)	ENSP00000508568.1:n.*690A>C
ENST00000692768.1:c.*162A>C (KRAS)	ENSP00000510254.1:n.*162A>C
ENST00000693229.1:c.*162A>C (KRAS)	ENSP00000509223.1:n.*162A>C
ENST00000256078.10:c.*283A>C (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*283A>C
ENST00000311936.8:c.*162A>C (KRAS) MANE Select	ENSP00000308495.3:n.*162A>C
ENST00000553788.6:c.*370T>G (ETFRF1)	ENSP00000451938.2:n.*370T>G
ENST00000256078.8:c.*283A>C (KRAS)	ENSP00000256078.4:n.*283A>C
ENST00000311936.7:c.*162A>C (KRAS)	ENSP00000308495.3:n.*162A>C
ENST00000553788.5:c.*370T>G (ETFRF1)	ENSP00000451938.1:n.*370T>G
ENST00000557334.5:c.*162A>C (KRAS)	ENSP00000452512.1:n.*162A>C
NM_004985.4:c.*162A>C (KRAS)	NP_004976.2:n.*162A>C
NM_033360.3:c.*283A>C (KRAS)	NP_203524.1:n.*283A>C
XM_011520653.1:c.*162A>C (KRAS)	XP_011518955.1:n.*162A>C
XM_011520653.3:c.*162A>C (KRAS)	XP_011518955.1:n.*162A>C
NM_001369786.1:c.*283A>C (KRAS)	NP_001356715.1:n.*283A>C
NM_001369787.1:c.*162A>C (KRAS)	NP_001356716.1:n.*162A>C
NM_004985.5:c.*162A>C (KRAS) MANE Select	NP_004976.2:n.*162A>C
NM_033360.4:c.*283A>C (KRAS) MANE Plus Clinical	NP_203524.1:n.*283A>C