Canonical Allele Identifier: CA384148275

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362730T>G (hg19) ; chr12:g.25209796T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209796T>G , CM000674.2:g.25209796T>G	GRCh38
NC_000012.11:g.25362730T>G , CM000674.1:g.25362730T>G	GRCh37
NC_000012.10:g.25253997T>G	NCBI36
NG_007524.1:g.46125A>C
NG_007524.2:g.46208A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.227A>C	ENSP00000452512.1:p.Ter76Ser
ENST00000685328.1:c.566A>C	ENSP00000508921.1:p.Ter189Ser
ENST00000686877.1:c.*537A>C	ENSP00000510431.1:n.*537A>C
ENST00000687356.1:c.*264A>C	ENSP00000510511.1:n.*264A>C
ENST00000688228.1:n.1040A>C
ENST00000688940.1:c.566A>C	ENSP00000509238.1:p.Ter189Ser
ENST00000690406.1:c.369A>C
ENST00000690804.1:c.*527A>C	ENSP00000508568.1:n.*527A>C
ENST00000692768.1:c.368A>C	ENSP00000510254.1:p.Ter123Ser
ENST00000693229.1:c.491A>C	ENSP00000509223.1:p.Ter164Ser
ENST00000256078.10:c.*120A>C MANE Plus Clinical	ENSP00000256078.5:n.*120A>C
ENST00000311936.8:c.566A>C MANE Select	ENSP00000308495.3:p.Ter189Ser
ENST00000256078.8:c.*120A>C	ENSP00000256078.4:n.*120A>C
ENST00000311936.7:c.566A>C	ENSP00000308495.3:p.Ter189Ser
ENST00000557334.5:c.227A>C	ENSP00000452512.1:p.Ter76Ser
NM_004985.4:c.566A>C	NP_004976.2:p.Ter189Ser
NM_033360.3:c.*120A>C	NP_203524.1:n.*120A>C
XM_011520653.1:c.566A>C	XP_011518955.1:p.Ter189Ser
XM_011520653.3:c.566A>C	XP_011518955.1:p.Ter189Ser
NM_001369786.1:c.*120A>C	NP_001356715.1:n.*120A>C
NM_001369787.1:c.566A>C	NP_001356716.1:p.Ter189Ser
NM_004985.5:c.566A>C MANE Select	NP_004976.2:p.Ter189Ser
NM_033360.4:c.*120A>C MANE Plus Clinical	NP_203524.1:n.*120A>C