Canonical Allele Identifier: CA2617994378

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209784-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209785del , CM000674.2:g.25209785del	GRCh38
NC_000012.11:g.25362719del , CM000674.1:g.25362719del	GRCh37
NC_000012.10:g.25253986del	NCBI36
NG_007524.1:g.46136del
NG_007524.2:g.46219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*10del	ENSP00000452512.1:n.*10del
ENST00000685328.1:c.*10del	ENSP00000508921.1:n.*10del
ENST00000686877.1:c.*548del	ENSP00000510431.1:n.*548del
ENST00000687356.1:c.*275del	ENSP00000510511.1:n.*275del
ENST00000688228.1:n.1051del
ENST00000688940.1:c.*10del	ENSP00000509238.1:n.*10del
ENST00000690406.1:c.380del
ENST00000690804.1:c.*538del	ENSP00000508568.1:n.*538del
ENST00000692768.1:c.*10del	ENSP00000510254.1:n.*10del
ENST00000693229.1:c.*10del	ENSP00000509223.1:n.*10del
ENST00000256078.10:c.*131del MANE Plus Clinical	ENSP00000256078.5:n.*131del
ENST00000311936.8:c.*10del MANE Select	ENSP00000308495.3:n.*10del
ENST00000256078.8:c.*131del	ENSP00000256078.4:n.*131del
ENST00000311936.7:c.*10del	ENSP00000308495.3:n.*10del
ENST00000557334.5:c.*10del	ENSP00000452512.1:n.*10del
NM_004985.4:c.*10del	NP_004976.2:n.*10del
NM_033360.3:c.*131del	NP_203524.1:n.*131del
XM_011520653.1:c.*10del	XP_011518955.1:n.*10del
XM_011520653.3:c.*10del	XP_011518955.1:n.*10del
NM_001369786.1:c.*131del	NP_001356715.1:n.*131del
NM_001369787.1:c.*10del	NP_001356716.1:n.*10del
NM_004985.5:c.*10del MANE Select	NP_004976.2:n.*10del
NM_033360.4:c.*131del MANE Plus Clinical	NP_203524.1:n.*131del