Canonical Allele Identifier: CA10641654

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308094
• ClinVar RCV Id: RCV000286204 ; RCV000376103
• dbSNP Id: rs886049191
• MyVariant Identifiers: chr12:g.25360883del (hg19) ; chr12:g.25207949del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25207949del , CM000674.2:g.25207949del	GRCh38
NC_000012.11:g.25360883del , CM000674.1:g.25360883del	GRCh37
NC_000012.10:g.25252150del	NCBI36
NG_007524.1:g.47972del
NG_007524.2:g.48055del

Transcript Alleles

HGVS	Amino-acid change
ENST00000685328.1:c.*1846del (KRAS)	ENSP00000508921.1:n.*1846del
ENST00000686877.1:c.*2384del (KRAS)	ENSP00000510431.1:n.*2384del
ENST00000687356.1:c.*2111del (KRAS)	ENSP00000510511.1:n.*2111del
ENST00000688940.1:c.*1846del (KRAS)	ENSP00000509238.1:n.*1846del
ENST00000690406.1:c.2216del (KRAS)
ENST00000690804.1:c.*2374del (KRAS)	ENSP00000508568.1:n.*2374del
ENST00000692768.1:c.*1846del (KRAS)	ENSP00000510254.1:n.*1846del
ENST00000693229.1:c.*1846del (KRAS)	ENSP00000509223.1:n.*1846del
ENST00000256078.10:c.*1967del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1967del
ENST00000311936.8:c.*1846del (KRAS) MANE Select	ENSP00000308495.3:n.*1846del
ENST00000553788.6:c.52-1246del (ETFRF1)	ENSP00000451938.2:n.52-1246del
ENST00000311936.7:c.*1846del (KRAS)	ENSP00000308495.3:n.*1846del
ENST00000553788.5:c.46-1246del (ETFRF1)	ENSP00000451938.1:n.46-1246del
NM_004985.4:c.*1846del (KRAS)	NP_004976.2:n.*1846del
NM_033360.3:c.*1967del (KRAS)	NP_203524.1:n.*1967del
XM_011520653.1:c.*1846del (KRAS)	XP_011518955.1:n.*1846del
XM_011520653.3:c.*1846del (KRAS)	XP_011518955.1:n.*1846del
NM_001369786.1:c.*1967del (KRAS)	NP_001356715.1:n.*1967del
NM_001369787.1:c.*1846del (KRAS)	NP_001356716.1:n.*1846del
NM_004985.5:c.*1846del (KRAS) MANE Select	NP_004976.2:n.*1846del
NM_033360.4:c.*1967del (KRAS) MANE Plus Clinical	NP_203524.1:n.*1967del