Canonical Allele Identifier: CA2617994333

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209768-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209768G>A , CM000674.2:g.25209768G>A	GRCh38
NC_000012.11:g.25362702G>A , CM000674.1:g.25362702G>A	GRCh37
NC_000012.10:g.25253969G>A	NCBI36
NG_007524.1:g.46153C>T
NG_007524.2:g.46236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*27C>T	ENSP00000452512.1:n.*27C>T
ENST00000685328.1:c.*27C>T	ENSP00000508921.1:n.*27C>T
ENST00000686877.1:c.*565C>T	ENSP00000510431.1:n.*565C>T
ENST00000687356.1:c.*292C>T	ENSP00000510511.1:n.*292C>T
ENST00000688228.1:n.1068C>T
ENST00000688940.1:c.*27C>T	ENSP00000509238.1:n.*27C>T
ENST00000690406.1:c.397C>T
ENST00000690804.1:c.*555C>T	ENSP00000508568.1:n.*555C>T
ENST00000692768.1:c.*27C>T	ENSP00000510254.1:n.*27C>T
ENST00000693229.1:c.*27C>T	ENSP00000509223.1:n.*27C>T
ENST00000256078.10:c.*148C>T MANE Plus Clinical	ENSP00000256078.5:n.*148C>T
ENST00000311936.8:c.*27C>T MANE Select	ENSP00000308495.3:n.*27C>T
ENST00000256078.8:c.*148C>T	ENSP00000256078.4:n.*148C>T
ENST00000311936.7:c.*27C>T	ENSP00000308495.3:n.*27C>T
ENST00000557334.5:c.*27C>T	ENSP00000452512.1:n.*27C>T
NM_004985.4:c.*27C>T	NP_004976.2:n.*27C>T
NM_033360.3:c.*148C>T	NP_203524.1:n.*148C>T
XM_011520653.1:c.*27C>T	XP_011518955.1:n.*27C>T
XM_011520653.3:c.*27C>T	XP_011518955.1:n.*27C>T
NM_001369786.1:c.*148C>T	NP_001356715.1:n.*148C>T
NM_001369787.1:c.*27C>T	NP_001356716.1:n.*27C>T
NM_004985.5:c.*27C>T MANE Select	NP_004976.2:n.*27C>T
NM_033360.4:c.*148C>T MANE Plus Clinical	NP_203524.1:n.*148C>T