Canonical Allele Identifier: CA384148460

Gene: KRAS

Linked Data

• ClinVar Variation Id: 547512
• ClinVar RCV Id: RCV000659837
• dbSNP Id: rs1555192443
• gnomAD v4: 12-25209872-G-A
• MyVariant Identifiers: chr12:g.25362806G>A (hg19) ; chr12:g.25209872G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209872G>A , CM000674.2:g.25209872G>A	GRCh38
NC_000012.11:g.25362806G>A , CM000674.1:g.25362806G>A	GRCh37
NC_000012.10:g.25254073G>A	NCBI36
NG_007524.1:g.46049C>T
NG_007524.2:g.46132C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.151C>T	ENSP00000452512.1:p.Arg51Ter
ENST00000685328.1:c.490C>T	ENSP00000508921.1:p.Arg164Ter
ENST00000686877.1:c.*461C>T	ENSP00000510431.1:n.*461C>T
ENST00000687356.1:c.*188C>T	ENSP00000510511.1:n.*188C>T
ENST00000688228.1:n.964C>T
ENST00000688940.1:c.490C>T	ENSP00000509238.1:p.Arg164Ter
ENST00000690406.1:c.293C>T
ENST00000690804.1:c.*451C>T	ENSP00000508568.1:n.*451C>T
ENST00000692768.1:c.292C>T	ENSP00000510254.1:p.Arg98Ter
ENST00000693229.1:c.415C>T	ENSP00000509223.1:p.Arg139Ter
ENST00000256078.10:c.*44C>T MANE Plus Clinical	ENSP00000256078.5:n.*44C>T
ENST00000311936.8:c.490C>T MANE Select	ENSP00000308495.3:p.Arg164Ter
ENST00000256078.8:c.*44C>T	ENSP00000256078.4:n.*44C>T
ENST00000311936.7:c.490C>T	ENSP00000308495.3:p.Arg164Ter
ENST00000557334.5:c.151C>T	ENSP00000452512.1:p.Arg51Ter
NM_004985.4:c.490C>T	NP_004976.2:p.Arg164Ter
NM_033360.3:c.*44C>T	NP_203524.1:n.*44C>T
XM_006719069.2:c.*44C>T	XP_006719132.1:n.*44C>T
XM_011520653.1:c.490C>T	XP_011518955.1:p.Arg164Ter
XM_006719069.4:c.*44C>T	XP_006719132.1:n.*44C>T
XM_011520653.3:c.490C>T	XP_011518955.1:p.Arg164Ter
NM_001369786.1:c.*44C>T	NP_001356715.1:n.*44C>T
NM_001369787.1:c.490C>T	NP_001356716.1:p.Arg164Ter
NM_004985.5:c.490C>T MANE Select	NP_004976.2:p.Arg164Ter
NM_033360.4:c.*44C>T MANE Plus Clinical	NP_203524.1:n.*44C>T