Canonical Allele Identifier: CA384148507

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362828G>T (hg19) ; chr12:g.25209894G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209894G>T , CM000674.2:g.25209894G>T	GRCh38
NC_000012.11:g.25362828G>T , CM000674.1:g.25362828G>T	GRCh37
NC_000012.10:g.25254095G>T	NCBI36
NG_007524.1:g.46027C>A
NG_007524.2:g.46110C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.129C>A	ENSP00000452512.1:p.Phe43Leu
ENST00000685328.1:c.468C>A	ENSP00000508921.1:p.Phe156Leu
ENST00000686877.1:c.*439C>A	ENSP00000510431.1:n.*439C>A
ENST00000687356.1:c.*166C>A	ENSP00000510511.1:n.*166C>A
ENST00000688228.1:n.942C>A
ENST00000688940.1:c.468C>A	ENSP00000509238.1:p.Phe156Leu
ENST00000690406.1:c.271C>A
ENST00000690804.1:c.*429C>A	ENSP00000508568.1:n.*429C>A
ENST00000692768.1:c.270C>A	ENSP00000510254.1:p.Phe90Leu
ENST00000693229.1:c.393C>A	ENSP00000509223.1:p.Phe131Leu
ENST00000256078.10:c.*22C>A MANE Plus Clinical	ENSP00000256078.5:n.*22C>A
ENST00000311936.8:c.468C>A MANE Select	ENSP00000308495.3:p.Phe156Leu
ENST00000256078.8:c.*22C>A	ENSP00000256078.4:n.*22C>A
ENST00000311936.7:c.468C>A	ENSP00000308495.3:p.Phe156Leu
ENST00000557334.5:c.129C>A	ENSP00000452512.1:p.Phe43Leu
NM_004985.4:c.468C>A	NP_004976.2:p.Phe156Leu
NM_033360.3:c.*22C>A	NP_203524.1:n.*22C>A
XM_006719069.2:c.*22C>A	XP_006719132.1:n.*22C>A
XM_011520653.1:c.468C>A	XP_011518955.1:p.Phe156Leu
XM_006719069.4:c.*22C>A	XP_006719132.1:n.*22C>A
XM_011520653.3:c.468C>A	XP_011518955.1:p.Phe156Leu
NM_001369786.1:c.*22C>A	NP_001356715.1:n.*22C>A
NM_001369787.1:c.468C>A	NP_001356716.1:p.Phe156Leu
NM_004985.5:c.468C>A MANE Select	NP_004976.2:p.Phe156Leu
NM_033360.4:c.*22C>A MANE Plus Clinical	NP_203524.1:n.*22C>A