Canonical Allele Identifier: CA603691349

Gene: KRAS

Linked Data

• dbSNP Id: rs1169144839
• gnomAD v2: 12-25362790-TTTTC-T
• gnomAD v4: 12-25209856-TTTTC-T
• MyVariant Identifiers: chr12:g.25362791_25362794del (hg19) ; chr12:g.25209857_25209860del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209860_25209863del , CM000674.2:g.25209860_25209863del	GRCh38
NC_000012.11:g.25362794_25362797del , CM000674.1:g.25362794_25362797del	GRCh37
NC_000012.10:g.25254061_25254064del	NCBI36
NG_007524.1:g.46061_46064del
NG_007524.2:g.46144_46147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.163_166del	ENSP00000452512.1:p.Glu55ArgfsTer2
ENST00000685328.1:c.502_505del	ENSP00000508921.1:p.Glu168ArgfsTer2
ENST00000686877.1:c.*473_*476del	ENSP00000510431.1:n.*473_*476del
ENST00000687356.1:c.*200_*203del	ENSP00000510511.1:n.*200_*203del
ENST00000688228.1:n.976_979del
ENST00000688940.1:c.502_505del	ENSP00000509238.1:p.Glu168ArgfsTer2
ENST00000690406.1:c.305_308del
ENST00000690804.1:c.*463_*466del	ENSP00000508568.1:n.*463_*466del
ENST00000692768.1:c.304_307del	ENSP00000510254.1:p.Glu102ArgfsTer2
ENST00000693229.1:c.427_430del	ENSP00000509223.1:p.Glu143ArgfsTer2
ENST00000256078.10:c.*56_*59del MANE Plus Clinical	ENSP00000256078.5:n.*56_*59del
ENST00000311936.8:c.502_505del MANE Select	ENSP00000308495.3:p.Glu168ArgfsTer2
ENST00000256078.8:c.*56_*59del	ENSP00000256078.4:n.*56_*59del
ENST00000311936.7:c.502_505del	ENSP00000308495.3:p.Glu168ArgfsTer2
ENST00000557334.5:c.163_166del	ENSP00000452512.1:p.Glu55ArgfsTer2
NM_004985.4:c.502_505del	NP_004976.2:p.Glu168ArgfsTer2
NM_033360.3:c.*56_*59del	NP_203524.1:n.*56_*59del
XM_006719069.2:c.*56_*59del	XP_006719132.1:n.*56_*59del
XM_011520653.1:c.502_505del	XP_011518955.1:p.Glu168ArgfsTer2
XM_006719069.4:c.*56_*59del	XP_006719132.1:n.*56_*59del
XM_011520653.3:c.502_505del	XP_011518955.1:p.Glu168ArgfsTer2
NM_001369786.1:c.*56_*59del	NP_001356715.1:n.*56_*59del
NM_001369787.1:c.502_505del	NP_001356716.1:p.Glu168ArgfsTer2
NM_004985.5:c.502_505del MANE Select	NP_004976.2:p.Glu168ArgfsTer2
NM_033360.4:c.*56_*59del MANE Plus Clinical	NP_203524.1:n.*56_*59del