Canonical Allele Identifier: CA2562170122

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209679-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209679C>A , CM000674.2:g.25209679C>A	GRCh38
NC_000012.11:g.25362613C>A , CM000674.1:g.25362613C>A	GRCh37
NC_000012.10:g.25253880C>A	NCBI36
NG_007524.1:g.46242G>T
NG_007524.2:g.46325G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*116G>T	ENSP00000452512.1:n.*116G>T
ENST00000685328.1:c.*116G>T	ENSP00000508921.1:n.*116G>T
ENST00000686877.1:c.*654G>T	ENSP00000510431.1:n.*654G>T
ENST00000687356.1:c.*381G>T	ENSP00000510511.1:n.*381G>T
ENST00000688228.1:n.1157G>T
ENST00000688940.1:c.*116G>T	ENSP00000509238.1:n.*116G>T
ENST00000690406.1:c.486G>T
ENST00000690804.1:c.*644G>T	ENSP00000508568.1:n.*644G>T
ENST00000692768.1:c.*116G>T	ENSP00000510254.1:n.*116G>T
ENST00000693229.1:c.*116G>T	ENSP00000509223.1:n.*116G>T
ENST00000256078.10:c.*237G>T MANE Plus Clinical	ENSP00000256078.5:n.*237G>T
ENST00000311936.8:c.*116G>T MANE Select	ENSP00000308495.3:n.*116G>T
ENST00000256078.8:c.*237G>T	ENSP00000256078.4:n.*237G>T
ENST00000311936.7:c.*116G>T	ENSP00000308495.3:n.*116G>T
ENST00000557334.5:c.*116G>T	ENSP00000452512.1:n.*116G>T
NM_004985.4:c.*116G>T	NP_004976.2:n.*116G>T
NM_033360.3:c.*237G>T	NP_203524.1:n.*237G>T
XM_011520653.1:c.*116G>T	XP_011518955.1:n.*116G>T
XM_011520653.3:c.*116G>T	XP_011518955.1:n.*116G>T
NM_001369786.1:c.*237G>T	NP_001356715.1:n.*237G>T
NM_001369787.1:c.*116G>T	NP_001356716.1:n.*116G>T
NM_004985.5:c.*116G>T MANE Select	NP_004976.2:n.*116G>T
NM_033360.4:c.*237G>T MANE Plus Clinical	NP_203524.1:n.*237G>T