Canonical Allele Identifier: CA2617994201

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209647-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209651del , CM000674.2:g.25209651del	GRCh38
NC_000012.11:g.25362585del , CM000674.1:g.25362585del	GRCh37
NC_000012.10:g.25253852del	NCBI36
NG_007524.1:g.46273del
NG_007524.2:g.46356del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*147del	ENSP00000452512.1:n.*147del
ENST00000685328.1:c.*147del	ENSP00000508921.1:n.*147del
ENST00000686877.1:c.*685del	ENSP00000510431.1:n.*685del
ENST00000687356.1:c.*412del	ENSP00000510511.1:n.*412del
ENST00000688940.1:c.*147del	ENSP00000509238.1:n.*147del
ENST00000690406.1:c.517del
ENST00000690804.1:c.*675del	ENSP00000508568.1:n.*675del
ENST00000692768.1:c.*147del	ENSP00000510254.1:n.*147del
ENST00000693229.1:c.*147del	ENSP00000509223.1:n.*147del
ENST00000256078.10:c.*268del MANE Plus Clinical	ENSP00000256078.5:n.*268del
ENST00000311936.8:c.*147del MANE Select	ENSP00000308495.3:n.*147del
ENST00000256078.8:c.*268del	ENSP00000256078.4:n.*268del
ENST00000311936.7:c.*147del	ENSP00000308495.3:n.*147del
ENST00000557334.5:c.*147del	ENSP00000452512.1:n.*147del
NM_004985.4:c.*147del	NP_004976.2:n.*147del
NM_033360.3:c.*268del	NP_203524.1:n.*268del
XM_011520653.1:c.*147del	XP_011518955.1:n.*147del
XM_011520653.3:c.*147del	XP_011518955.1:n.*147del
NM_001369786.1:c.*268del	NP_001356715.1:n.*268del
NM_001369787.1:c.*147del	NP_001356716.1:n.*147del
NM_004985.5:c.*147del MANE Select	NP_004976.2:n.*147del
NM_033360.4:c.*268del MANE Plus Clinical	NP_203524.1:n.*268del