Canonical Allele Identifier: CA2617994327

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209760-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209760A>G , CM000674.2:g.25209760A>G	GRCh38
NC_000012.11:g.25362694A>G , CM000674.1:g.25362694A>G	GRCh37
NC_000012.10:g.25253961A>G	NCBI36
NG_007524.1:g.46161T>C
NG_007524.2:g.46244T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*35T>C	ENSP00000452512.1:n.*35T>C
ENST00000685328.1:c.*35T>C	ENSP00000508921.1:n.*35T>C
ENST00000686877.1:c.*573T>C	ENSP00000510431.1:n.*573T>C
ENST00000687356.1:c.*300T>C	ENSP00000510511.1:n.*300T>C
ENST00000688228.1:n.1076T>C
ENST00000688940.1:c.*35T>C	ENSP00000509238.1:n.*35T>C
ENST00000690406.1:c.405T>C
ENST00000690804.1:c.*563T>C	ENSP00000508568.1:n.*563T>C
ENST00000692768.1:c.*35T>C	ENSP00000510254.1:n.*35T>C
ENST00000693229.1:c.*35T>C	ENSP00000509223.1:n.*35T>C
ENST00000256078.10:c.*156T>C MANE Plus Clinical	ENSP00000256078.5:n.*156T>C
ENST00000311936.8:c.*35T>C MANE Select	ENSP00000308495.3:n.*35T>C
ENST00000256078.8:c.*156T>C	ENSP00000256078.4:n.*156T>C
ENST00000311936.7:c.*35T>C	ENSP00000308495.3:n.*35T>C
ENST00000557334.5:c.*35T>C	ENSP00000452512.1:n.*35T>C
NM_004985.4:c.*35T>C	NP_004976.2:n.*35T>C
NM_033360.3:c.*156T>C	NP_203524.1:n.*156T>C
XM_011520653.1:c.*35T>C	XP_011518955.1:n.*35T>C
XM_011520653.3:c.*35T>C	XP_011518955.1:n.*35T>C
NM_001369786.1:c.*156T>C	NP_001356715.1:n.*156T>C
NM_001369787.1:c.*35T>C	NP_001356716.1:n.*35T>C
NM_004985.5:c.*35T>C MANE Select	NP_004976.2:n.*35T>C
NM_033360.4:c.*156T>C MANE Plus Clinical	NP_203524.1:n.*156T>C