Canonical Allele Identifier: CA2580085348

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1711000
• ClinVar RCV Id: RCV002292287
• gnomAD v4: 12-25245403-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245403T>G , CM000674.2:g.25245403T>G	GRCh38
NC_000012.11:g.25398337T>G , CM000674.1:g.25398337T>G	GRCh37
NC_000012.10:g.25289604T>G	NCBI36
NG_007524.1:g.10518A>C
NG_007524.2:g.10601A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.-11-8A>C	ENSP00000451856.1:n.-11-8A>C
ENST00000557334.6:c.-11-8A>C	ENSP00000452512.1:n.-11-8A>C
ENST00000685328.1:c.-11-8A>C	ENSP00000508921.1:n.-11-8A>C
ENST00000686877.1:c.-11-8A>C	ENSP00000510431.1:n.-11-8A>C
ENST00000686969.1:c.-11-8A>C	ENSP00000510479.1:n.-11-8A>C
ENST00000687356.1:c.-11-8A>C	ENSP00000510511.1:n.-11-8A>C
ENST00000688940.1:c.-11-8A>C	ENSP00000509238.1:n.-11-8A>C
ENST00000690804.1:c.-11-8A>C	ENSP00000508568.1:n.-11-8A>C
ENST00000692768.1:c.-88+5348A>C	ENSP00000510254.1:n.-88+5348A>C
ENST00000693229.1:c.-11-8A>C	ENSP00000509223.1:n.-11-8A>C
ENST00000256078.10:c.-11-8A>C MANE Plus Clinical	ENSP00000256078.5:n.-11-8A>C
ENST00000311936.8:c.-11-8A>C MANE Select	ENSP00000308495.3:n.-11-8A>C
ENST00000256078.8:c.-11-8A>C	ENSP00000256078.4:n.-11-8A>C
ENST00000311936.7:c.-11-8A>C	ENSP00000308495.3:n.-11-8A>C
ENST00000556131.1:c.-11-8A>C	ENSP00000451856.1:n.-11-8A>C
ENST00000557334.5:c.-11-8A>C	ENSP00000452512.1:n.-11-8A>C
NM_004985.4:c.-11-8A>C	NP_004976.2:n.-11-8A>C
NM_033360.3:c.-11-8A>C	NP_203524.1:n.-11-8A>C
XM_006719069.2:c.-11-8A>C	XP_006719132.1:n.-11-8A>C
XM_011520653.1:c.-11-8A>C	XP_011518955.1:n.-11-8A>C
XM_006719069.4:c.-11-8A>C	XP_006719132.1:n.-11-8A>C
XM_011520653.3:c.-11-8A>C	XP_011518955.1:n.-11-8A>C
NM_001369786.1:c.-11-8A>C	NP_001356715.1:n.-11-8A>C
NM_001369787.1:c.-11-8A>C	NP_001356716.1:n.-11-8A>C
NM_004985.5:c.-11-8A>C MANE Select	NP_004976.2:n.-11-8A>C
NM_033360.4:c.-11-8A>C MANE Plus Clinical	NP_203524.1:n.-11-8A>C