Canonical Allele Identifier: CA645572083

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209898-GCAT-G
• COSMIC: COSM1360823

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209904_25209906del , CM000674.2:g.25209904_25209906del	GRCh38
NC_000012.11:g.25362838_25362840del , CM000674.1:g.25362838_25362840del	GRCh37
NC_000012.10:g.25254105_25254107del	NCBI36
NG_007524.1:g.46020_46022del
NG_007524.2:g.46103_46105del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.122_124del	ENSP00000452512.1:p.Asp41del
ENST00000685328.1:c.461_463del	ENSP00000508921.1:p.Asp154del
ENST00000686877.1:c.*432_*434del	ENSP00000510431.1:n.*432_*434del
ENST00000687356.1:c.*159_*161del	ENSP00000510511.1:n.*159_*161del
ENST00000688228.1:n.935_937del
ENST00000688940.1:c.461_463del	ENSP00000509238.1:p.Asp154del
ENST00000690406.1:c.264_266del
ENST00000690804.1:c.*422_*424del	ENSP00000508568.1:n.*422_*424del
ENST00000692768.1:c.263_265del	ENSP00000510254.1:p.Asp88del
ENST00000693229.1:c.386_388del	ENSP00000509223.1:p.Asp129del
ENST00000256078.10:c.*15_*17del MANE Plus Clinical	ENSP00000256078.5:n.*15_*17del
ENST00000311936.8:c.461_463del MANE Select	ENSP00000308495.3:p.Asp154del
ENST00000256078.8:c.*15_*17del	ENSP00000256078.4:n.*15_*17del
ENST00000311936.7:c.461_463del	ENSP00000308495.3:p.Asp154del
ENST00000557334.5:c.122_124del	ENSP00000452512.1:p.Asp41del
NM_004985.4:c.461_463del	NP_004976.2:p.Asp154del
NM_033360.3:c.*15_*17del	NP_203524.1:n.*15_*17del
XM_006719069.2:c.*15_*17del	XP_006719132.1:n.*15_*17del
XM_011520653.1:c.461_463del	XP_011518955.1:p.Asp154del
XM_006719069.4:c.*15_*17del	XP_006719132.1:n.*15_*17del
XM_011520653.3:c.461_463del	XP_011518955.1:p.Asp154del
NM_001369786.1:c.*15_*17del	NP_001356715.1:n.*15_*17del
NM_001369787.1:c.461_463del	NP_001356716.1:p.Asp154del
NM_004985.5:c.461_463del MANE Select	NP_004976.2:p.Asp154del
NM_033360.4:c.*15_*17del MANE Plus Clinical	NP_203524.1:n.*15_*17del