Canonical Allele Identifier: CA384151742

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25380186T>A (hg19) ; chr12:g.25227252T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227252T>A , CM000674.2:g.25227252T>A	GRCh38
NC_000012.11:g.25380186T>A , CM000674.1:g.25380186T>A	GRCh37
NC_000012.10:g.25271453T>A	NCBI36
NG_007524.1:g.28669A>T
NG_007524.2:g.28752A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17341A>T	ENSP00000452512.1:n.112-17341A>T
ENST00000685328.1:c.272A>T	ENSP00000508921.1:p.Glu91Val
ENST00000686877.1:c.*243A>T	ENSP00000510431.1:n.*243A>T
ENST00000687356.1:c.112-1479A>T	ENSP00000510511.1:n.112-1479A>T
ENST00000688228.1:n.746A>T
ENST00000688940.1:c.272A>T	ENSP00000509238.1:p.Glu91Val
ENST00000690804.1:c.*233A>T	ENSP00000508568.1:n.*233A>T
ENST00000692768.1:c.74A>T	ENSP00000510254.1:p.Glu25Val
ENST00000693229.1:c.197A>T	ENSP00000509223.1:p.Glu66Val
ENST00000256078.10:c.272A>T MANE Plus Clinical	ENSP00000256078.5:p.Glu91Val
ENST00000311936.8:c.272A>T MANE Select	ENSP00000308495.3:p.Glu91Val
ENST00000256078.8:c.272A>T	ENSP00000256078.4:p.Glu91Val
ENST00000311936.7:c.272A>T	ENSP00000308495.3:p.Glu91Val
ENST00000557334.5:c.112-17341A>T	ENSP00000452512.1:n.112-17341A>T
NM_004985.4:c.272A>T	NP_004976.2:p.Glu91Val
NM_033360.3:c.272A>T	NP_203524.1:p.Glu91Val
XM_006719069.2:c.272A>T	XP_006719132.1:p.Glu91Val
XM_011520653.1:c.272A>T	XP_011518955.1:p.Glu91Val
XM_006719069.4:c.272A>T	XP_006719132.1:p.Glu91Val
XM_011520653.3:c.272A>T	XP_011518955.1:p.Glu91Val
NM_001369786.1:c.272A>T	NP_001356715.1:p.Glu91Val
NM_001369787.1:c.272A>T	NP_001356716.1:p.Glu91Val
NM_004985.5:c.272A>T MANE Select	NP_004976.2:p.Glu91Val
NM_033360.4:c.272A>T MANE Plus Clinical	NP_203524.1:p.Glu91Val