Canonical Allele Identifier: CA246093

Gene: KRAS

Linked Data

• ClinVar Variation Id: 197769
• ClinVar RCV Id: RCV000218179 ; RCV000724550 ; RCV002517746
• dbSNP Id: rs794727720
• MyVariant Identifiers: chr12:g.25362826T>C (hg19) ; chr12:g.25209892T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209892T>C , CM000674.2:g.25209892T>C	GRCh38
NC_000012.11:g.25362826T>C , CM000674.1:g.25362826T>C	GRCh37
NC_000012.10:g.25254093T>C	NCBI36
NG_007524.1:g.46029A>G
NG_007524.2:g.46112A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.131A>G	ENSP00000452512.1:p.Tyr44Cys
ENST00000685328.1:c.470A>G	ENSP00000508921.1:p.Tyr157Cys
ENST00000686877.1:c.*441A>G	ENSP00000510431.1:n.*441A>G
ENST00000687356.1:c.*168A>G	ENSP00000510511.1:n.*168A>G
ENST00000688228.1:n.944A>G
ENST00000688940.1:c.470A>G	ENSP00000509238.1:p.Tyr157Cys
ENST00000690406.1:c.273A>G
ENST00000690804.1:c.*431A>G	ENSP00000508568.1:n.*431A>G
ENST00000692768.1:c.272A>G	ENSP00000510254.1:p.Tyr91Cys
ENST00000693229.1:c.395A>G	ENSP00000509223.1:p.Tyr132Cys
ENST00000256078.10:c.*24A>G MANE Plus Clinical	ENSP00000256078.5:n.*24A>G
ENST00000311936.8:c.470A>G MANE Select	ENSP00000308495.3:p.Tyr157Cys
ENST00000256078.8:c.*24A>G	ENSP00000256078.4:n.*24A>G
ENST00000311936.7:c.470A>G	ENSP00000308495.3:p.Tyr157Cys
ENST00000557334.5:c.131A>G	ENSP00000452512.1:p.Tyr44Cys
NM_004985.4:c.470A>G	NP_004976.2:p.Tyr157Cys
NM_033360.3:c.*24A>G	NP_203524.1:n.*24A>G
XM_006719069.2:c.*24A>G	XP_006719132.1:n.*24A>G
XM_011520653.1:c.470A>G	XP_011518955.1:p.Tyr157Cys
XM_006719069.4:c.*24A>G	XP_006719132.1:n.*24A>G
XM_011520653.3:c.470A>G	XP_011518955.1:p.Tyr157Cys
NM_001369786.1:c.*24A>G	NP_001356715.1:n.*24A>G
NM_001369787.1:c.470A>G	NP_001356716.1:p.Tyr157Cys
NM_004985.5:c.470A>G MANE Select	NP_004976.2:p.Tyr157Cys
NM_033360.4:c.*24A>G MANE Plus Clinical	NP_203524.1:n.*24A>G