Canonical Allele Identifier: CA384151476

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378651T>A (hg19) ; chr12:g.25225717T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225717T>A , CM000674.2:g.25225717T>A	GRCh38
NC_000012.11:g.25378651T>A , CM000674.1:g.25378651T>A	GRCh37
NC_000012.10:g.25269918T>A	NCBI36
NG_007524.1:g.30204A>T
NG_007524.2:g.30287A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15806A>T	ENSP00000452512.1:n.112-15806A>T
ENST00000685328.1:c.347A>T	ENSP00000508921.1:p.Asn116Ile
ENST00000686877.1:c.*318A>T	ENSP00000510431.1:n.*318A>T
ENST00000687356.1:c.*45A>T	ENSP00000510511.1:n.*45A>T
ENST00000688228.1:n.821A>T
ENST00000688940.1:c.347A>T	ENSP00000509238.1:p.Asn116Ile
ENST00000690406.1:c.57A>T
ENST00000690804.1:c.*308A>T	ENSP00000508568.1:n.*308A>T
ENST00000692768.1:c.149A>T	ENSP00000510254.1:p.Asn50Ile
ENST00000693229.1:c.272A>T	ENSP00000509223.1:p.Asn91Ile
ENST00000256078.10:c.347A>T MANE Plus Clinical	ENSP00000256078.5:p.Asn116Ile
ENST00000311936.8:c.347A>T MANE Select	ENSP00000308495.3:p.Asn116Ile
ENST00000256078.8:c.347A>T	ENSP00000256078.4:p.Asn116Ile
ENST00000311936.7:c.347A>T	ENSP00000308495.3:p.Asn116Ile
ENST00000557334.5:c.112-15806A>T	ENSP00000452512.1:n.112-15806A>T
NM_004985.4:c.347A>T	NP_004976.2:p.Asn116Ile
NM_033360.3:c.347A>T	NP_203524.1:p.Asn116Ile
XM_006719069.2:c.347A>T	XP_006719132.1:p.Asn116Ile
XM_011520653.1:c.347A>T	XP_011518955.1:p.Asn116Ile
XM_006719069.4:c.347A>T	XP_006719132.1:p.Asn116Ile
XM_011520653.3:c.347A>T	XP_011518955.1:p.Asn116Ile
NM_001369786.1:c.347A>T	NP_001356715.1:p.Asn116Ile
NM_001369787.1:c.347A>T	NP_001356716.1:p.Asn116Ile
NM_004985.5:c.347A>T MANE Select	NP_004976.2:p.Asn116Ile
NM_033360.4:c.347A>T MANE Plus Clinical	NP_203524.1:p.Asn116Ile