Canonical Allele Identifier: CA6486818

Gene: KRAS

Linked Data

• dbSNP Id: rs777982714
• ExAC: 12:25362702 GC / G
• gnomAD v2: 12-25362702-GC-G
• gnomAD v4: 12-25209768-GC-G
• MyVariant Identifiers: chr12:g.25362703del (hg19) ; chr12:g.25209769del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209770del , CM000674.2:g.25209770del	GRCh38
NC_000012.11:g.25362704del , CM000674.1:g.25362704del	GRCh37
NC_000012.10:g.25253971del	NCBI36
NG_007524.1:g.46152del
NG_007524.2:g.46235del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*26del	ENSP00000452512.1:n.*26del
ENST00000685328.1:c.*26del	ENSP00000508921.1:n.*26del
ENST00000686877.1:c.*564del	ENSP00000510431.1:n.*564del
ENST00000687356.1:c.*291del	ENSP00000510511.1:n.*291del
ENST00000688228.1:n.1067del
ENST00000688940.1:c.*26del	ENSP00000509238.1:n.*26del
ENST00000690406.1:c.396del
ENST00000690804.1:c.*554del	ENSP00000508568.1:n.*554del
ENST00000692768.1:c.*26del	ENSP00000510254.1:n.*26del
ENST00000693229.1:c.*26del	ENSP00000509223.1:n.*26del
ENST00000256078.10:c.*147del MANE Plus Clinical	ENSP00000256078.5:n.*147del
ENST00000311936.8:c.*26del MANE Select	ENSP00000308495.3:n.*26del
ENST00000256078.8:c.*147del	ENSP00000256078.4:n.*147del
ENST00000311936.7:c.*26del	ENSP00000308495.3:n.*26del
ENST00000557334.5:c.*26del	ENSP00000452512.1:n.*26del
NM_004985.4:c.*26del	NP_004976.2:n.*26del
NM_033360.3:c.*147del	NP_203524.1:n.*147del
XM_011520653.1:c.*26del	XP_011518955.1:n.*26del
XM_011520653.3:c.*26del	XP_011518955.1:n.*26del
NM_001369786.1:c.*147del	NP_001356715.1:n.*147del
NM_001369787.1:c.*26del	NP_001356716.1:n.*26del
NM_004985.5:c.*26del MANE Select	NP_004976.2:n.*26del
NM_033360.4:c.*147del MANE Plus Clinical	NP_203524.1:n.*147del