Canonical Allele Identifier: CA384151444

Gene: KRAS

Linked Data

• dbSNP Id: rs2141506205
• MyVariant Identifiers: chr12:g.25378644A>T (hg19) ; chr12:g.25225710A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225710A>T , CM000674.2:g.25225710A>T	GRCh38
NC_000012.11:g.25378644A>T , CM000674.1:g.25378644A>T	GRCh37
NC_000012.10:g.25269911A>T	NCBI36
NG_007524.1:g.30211T>A
NG_007524.2:g.30294T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15799T>A	ENSP00000452512.1:n.112-15799T>A
ENST00000685328.1:c.354T>A	ENSP00000508921.1:p.Cys118Ter
ENST00000686877.1:c.*325T>A	ENSP00000510431.1:n.*325T>A
ENST00000687356.1:c.*52T>A	ENSP00000510511.1:n.*52T>A
ENST00000688228.1:n.828T>A
ENST00000688940.1:c.354T>A	ENSP00000509238.1:p.Cys118Ter
ENST00000690406.1:c.64T>A
ENST00000690804.1:c.*315T>A	ENSP00000508568.1:n.*315T>A
ENST00000692768.1:c.156T>A	ENSP00000510254.1:p.Cys52Ter
ENST00000693229.1:c.279T>A	ENSP00000509223.1:p.Cys93Ter
ENST00000256078.10:c.354T>A MANE Plus Clinical	ENSP00000256078.5:p.Cys118Ter
ENST00000311936.8:c.354T>A MANE Select	ENSP00000308495.3:p.Cys118Ter
ENST00000256078.8:c.354T>A	ENSP00000256078.4:p.Cys118Ter
ENST00000311936.7:c.354T>A	ENSP00000308495.3:p.Cys118Ter
ENST00000557334.5:c.112-15799T>A	ENSP00000452512.1:n.112-15799T>A
NM_004985.4:c.354T>A	NP_004976.2:p.Cys118Ter
NM_033360.3:c.354T>A	NP_203524.1:p.Cys118Ter
XM_006719069.2:c.354T>A	XP_006719132.1:p.Cys118Ter
XM_011520653.1:c.354T>A	XP_011518955.1:p.Cys118Ter
XM_006719069.4:c.354T>A	XP_006719132.1:p.Cys118Ter
XM_011520653.3:c.354T>A	XP_011518955.1:p.Cys118Ter
NM_001369786.1:c.354T>A	NP_001356715.1:p.Cys118Ter
NM_001369787.1:c.354T>A	NP_001356716.1:p.Cys118Ter
NM_004985.5:c.354T>A MANE Select	NP_004976.2:p.Cys118Ter
NM_033360.4:c.354T>A MANE Plus Clinical	NP_203524.1:p.Cys118Ter