Canonical Allele Identifier: CA384148295

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362739A>T (hg19) ; chr12:g.25209805A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209805A>T , CM000674.2:g.25209805A>T	GRCh38
NC_000012.11:g.25362739A>T , CM000674.1:g.25362739A>T	GRCh37
NC_000012.10:g.25254006A>T	NCBI36
NG_007524.1:g.46116T>A
NG_007524.2:g.46199T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.218T>A	ENSP00000452512.1:p.Val73Glu
ENST00000685328.1:c.557T>A	ENSP00000508921.1:p.Val186Glu
ENST00000686877.1:c.*528T>A	ENSP00000510431.1:n.*528T>A
ENST00000687356.1:c.*255T>A	ENSP00000510511.1:n.*255T>A
ENST00000688228.1:n.1031T>A
ENST00000688940.1:c.557T>A	ENSP00000509238.1:p.Val186Glu
ENST00000690406.1:c.360T>A
ENST00000690804.1:c.*518T>A	ENSP00000508568.1:n.*518T>A
ENST00000692768.1:c.359T>A	ENSP00000510254.1:p.Val120Glu
ENST00000693229.1:c.482T>A	ENSP00000509223.1:p.Val161Glu
ENST00000256078.10:c.*111T>A MANE Plus Clinical	ENSP00000256078.5:n.*111T>A
ENST00000311936.8:c.557T>A MANE Select	ENSP00000308495.3:p.Val186Glu
ENST00000256078.8:c.*111T>A	ENSP00000256078.4:n.*111T>A
ENST00000311936.7:c.557T>A	ENSP00000308495.3:p.Val186Glu
ENST00000557334.5:c.218T>A	ENSP00000452512.1:p.Val73Glu
NM_004985.4:c.557T>A	NP_004976.2:p.Val186Glu
NM_033360.3:c.*111T>A	NP_203524.1:n.*111T>A
XM_011520653.1:c.557T>A	XP_011518955.1:p.Val186Glu
XM_011520653.3:c.557T>A	XP_011518955.1:p.Val186Glu
NM_001369786.1:c.*111T>A	NP_001356715.1:n.*111T>A
NM_001369787.1:c.557T>A	NP_001356716.1:p.Val186Glu
NM_004985.5:c.557T>A MANE Select	NP_004976.2:p.Val186Glu
NM_033360.4:c.*111T>A MANE Plus Clinical	NP_203524.1:n.*111T>A