Canonical Allele Identifier: CA384151139

Gene: KRAS

Linked Data

• dbSNP Id: rs2141505698
• gnomAD v4: 12-25225642-A-T
• MyVariant Identifiers: chr12:g.25378576A>T (hg19) ; chr12:g.25225642A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225642A>T , CM000674.2:g.25225642A>T	GRCh38
NC_000012.11:g.25378576A>T , CM000674.1:g.25378576A>T	GRCh37
NC_000012.10:g.25269843A>T	NCBI36
NG_007524.1:g.30279T>A
NG_007524.2:g.30362T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-15731T>A	ENSP00000452512.1:n.112-15731T>A
ENST00000685328.1:c.422T>A	ENSP00000508921.1:p.Phe141Tyr
ENST00000686877.1:c.*393T>A	ENSP00000510431.1:n.*393T>A
ENST00000687356.1:c.*120T>A	ENSP00000510511.1:n.*120T>A
ENST00000688228.1:n.896T>A
ENST00000688940.1:c.422T>A	ENSP00000509238.1:p.Phe141Tyr
ENST00000690406.1:c.132T>A
ENST00000690804.1:c.*383T>A	ENSP00000508568.1:n.*383T>A
ENST00000692768.1:c.224T>A	ENSP00000510254.1:p.Phe75Tyr
ENST00000693229.1:c.347T>A	ENSP00000509223.1:p.Phe116Tyr
ENST00000256078.10:c.422T>A MANE Plus Clinical	ENSP00000256078.5:p.Phe141Tyr
ENST00000311936.8:c.422T>A MANE Select	ENSP00000308495.3:p.Phe141Tyr
ENST00000256078.8:c.422T>A	ENSP00000256078.4:p.Phe141Tyr
ENST00000311936.7:c.422T>A	ENSP00000308495.3:p.Phe141Tyr
ENST00000557334.5:c.112-15731T>A	ENSP00000452512.1:n.112-15731T>A
NM_004985.4:c.422T>A	NP_004976.2:p.Phe141Tyr
NM_033360.3:c.422T>A	NP_203524.1:p.Phe141Tyr
XM_006719069.2:c.422T>A	XP_006719132.1:p.Phe141Tyr
XM_011520653.1:c.422T>A	XP_011518955.1:p.Phe141Tyr
XM_006719069.4:c.422T>A	XP_006719132.1:p.Phe141Tyr
XM_011520653.3:c.422T>A	XP_011518955.1:p.Phe141Tyr
NM_001369786.1:c.422T>A	NP_001356715.1:p.Phe141Tyr
NM_001369787.1:c.422T>A	NP_001356716.1:p.Phe141Tyr
NM_004985.5:c.422T>A MANE Select	NP_004976.2:p.Phe141Tyr
NM_033360.4:c.422T>A MANE Plus Clinical	NP_203524.1:p.Phe141Tyr