Canonical Allele Identifier: CA6486825

Gene: KRAS

Linked Data

• ClinVar Variation Id: 2697277
• ClinVar RCV Id: RCV003539524
• dbSNP Id: rs750905218
• ExAC: 12:25362789 C / T
• gnomAD v2: 12-25362789-C-T
• gnomAD v4: 12-25209855-C-T
• MyVariant Identifiers: chr12:g.25362789C>T (hg19) ; chr12:g.25209855C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209855C>T , CM000674.2:g.25209855C>T	GRCh38
NC_000012.11:g.25362789C>T , CM000674.1:g.25362789C>T	GRCh37
NC_000012.10:g.25254056C>T	NCBI36
NG_007524.1:g.46066G>A
NG_007524.2:g.46149G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.168G>A	ENSP00000452512.1:p.Lys56=
ENST00000685328.1:c.507G>A	ENSP00000508921.1:p.Lys169=
ENST00000686877.1:c.*478G>A	ENSP00000510431.1:n.*478G>A
ENST00000687356.1:c.*205G>A	ENSP00000510511.1:n.*205G>A
ENST00000688228.1:n.981G>A
ENST00000688940.1:c.507G>A	ENSP00000509238.1:p.Lys169=
ENST00000690406.1:c.310G>A
ENST00000690804.1:c.*468G>A	ENSP00000508568.1:n.*468G>A
ENST00000692768.1:c.309G>A	ENSP00000510254.1:p.Lys103=
ENST00000693229.1:c.432G>A	ENSP00000509223.1:p.Lys144=
ENST00000256078.10:c.*61G>A MANE Plus Clinical	ENSP00000256078.5:n.*61G>A
ENST00000311936.8:c.507G>A MANE Select	ENSP00000308495.3:p.Lys169=
ENST00000256078.8:c.*61G>A	ENSP00000256078.4:n.*61G>A
ENST00000311936.7:c.507G>A	ENSP00000308495.3:p.Lys169=
ENST00000557334.5:c.168G>A	ENSP00000452512.1:p.Lys56=
NM_004985.4:c.507G>A	NP_004976.2:p.Lys169=
NM_033360.3:c.*61G>A	NP_203524.1:n.*61G>A
XM_006719069.2:c.*61G>A	XP_006719132.1:n.*61G>A
XM_011520653.1:c.507G>A	XP_011518955.1:p.Lys169=
XM_006719069.4:c.*61G>A	XP_006719132.1:n.*61G>A
XM_011520653.3:c.507G>A	XP_011518955.1:p.Lys169=
NM_001369786.1:c.*61G>A	NP_001356715.1:n.*61G>A
NM_001369787.1:c.507G>A	NP_001356716.1:p.Lys169=
NM_004985.5:c.507G>A MANE Select	NP_004976.2:p.Lys169=
NM_033360.4:c.*61G>A MANE Plus Clinical	NP_203524.1:n.*61G>A