Canonical Allele Identifier: CA384148307

Gene: KRAS

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209809A>T , CM000674.2:g.25209809A>T	GRCh38
NC_000012.11:g.25362743A>T , CM000674.1:g.25362743A>T	GRCh37
NC_000012.10:g.25254010A>T	NCBI36
NG_007524.1:g.46112T>A
NG_007524.2:g.46195T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.214T>A	ENSP00000452512.1:p.Cys72Ser
ENST00000685328.1:c.553T>A	ENSP00000508921.1:p.Cys185Ser
ENST00000686877.1:c.*524T>A	ENSP00000510431.1:n.*524T>A
ENST00000687356.1:c.*251T>A	ENSP00000510511.1:n.*251T>A
ENST00000688228.1:n.1027T>A
ENST00000688940.1:c.553T>A	ENSP00000509238.1:p.Cys185Ser
ENST00000690406.1:c.356T>A
ENST00000690804.1:c.*514T>A	ENSP00000508568.1:n.*514T>A
ENST00000692768.1:c.355T>A	ENSP00000510254.1:p.Cys119Ser
ENST00000693229.1:c.478T>A	ENSP00000509223.1:p.Cys160Ser
ENST00000256078.10:c.*107T>A MANE Plus Clinical	ENSP00000256078.5:n.*107T>A
ENST00000311936.8:c.553T>A MANE Select	ENSP00000308495.3:p.Cys185Ser
ENST00000256078.8:c.*107T>A	ENSP00000256078.4:n.*107T>A
ENST00000311936.7:c.553T>A	ENSP00000308495.3:p.Cys185Ser
ENST00000557334.5:c.214T>A	ENSP00000452512.1:p.Cys72Ser
NM_004985.4:c.553T>A	NP_004976.2:p.Cys185Ser
NM_033360.3:c.*107T>A	NP_203524.1:n.*107T>A
XM_011520653.1:c.553T>A	XP_011518955.1:p.Cys185Ser
XM_011520653.3:c.553T>A	XP_011518955.1:p.Cys185Ser
NM_001369786.1:c.*107T>A	NP_001356715.1:n.*107T>A
NM_001369787.1:c.553T>A	NP_001356716.1:p.Cys185Ser
NM_004985.5:c.553T>A MANE Select	NP_004976.2:p.Cys185Ser
NM_033360.4:c.*107T>A MANE Plus Clinical	NP_203524.1:n.*107T>A