Canonical Allele Identifier: CA234206805

Gene: KRAS

Linked Data

• dbSNP Id: rs564331329
• gnomAD v3: 12-25209706-A-C
• gnomAD v4: 12-25209706-A-C
• MyVariant Identifiers: chr12:g.25362640A>C (hg19) ; chr12:g.25209706A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209706A>C , CM000674.2:g.25209706A>C	GRCh38
NC_000012.11:g.25362640A>C , CM000674.1:g.25362640A>C	GRCh37
NC_000012.10:g.25253907A>C	NCBI36
NG_007524.1:g.46215T>G
NG_007524.2:g.46298T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*89T>G	ENSP00000452512.1:n.*89T>G
ENST00000685328.1:c.*89T>G	ENSP00000508921.1:n.*89T>G
ENST00000686877.1:c.*627T>G	ENSP00000510431.1:n.*627T>G
ENST00000687356.1:c.*354T>G	ENSP00000510511.1:n.*354T>G
ENST00000688228.1:n.1130T>G
ENST00000688940.1:c.*89T>G	ENSP00000509238.1:n.*89T>G
ENST00000690406.1:c.459T>G
ENST00000690804.1:c.*617T>G	ENSP00000508568.1:n.*617T>G
ENST00000692768.1:c.*89T>G	ENSP00000510254.1:n.*89T>G
ENST00000693229.1:c.*89T>G	ENSP00000509223.1:n.*89T>G
ENST00000256078.10:c.*210T>G MANE Plus Clinical	ENSP00000256078.5:n.*210T>G
ENST00000311936.8:c.*89T>G MANE Select	ENSP00000308495.3:n.*89T>G
ENST00000256078.8:c.*210T>G	ENSP00000256078.4:n.*210T>G
ENST00000311936.7:c.*89T>G	ENSP00000308495.3:n.*89T>G
ENST00000557334.5:c.*89T>G	ENSP00000452512.1:n.*89T>G
NM_004985.4:c.*89T>G	NP_004976.2:n.*89T>G
NM_033360.3:c.*210T>G	NP_203524.1:n.*210T>G
XM_011520653.1:c.*89T>G	XP_011518955.1:n.*89T>G
XM_011520653.3:c.*89T>G	XP_011518955.1:n.*89T>G
NM_001369786.1:c.*210T>G	NP_001356715.1:n.*210T>G
NM_001369787.1:c.*89T>G	NP_001356716.1:n.*89T>G
NM_004985.5:c.*89T>G MANE Select	NP_004976.2:n.*89T>G
NM_033360.4:c.*210T>G MANE Plus Clinical	NP_203524.1:n.*210T>G