Canonical Allele Identifier: CA478889998
Gene: KRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.25378563T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225629T>G , CM000674.2:g.25225629T>G GRCh38
NC_000012.11:g.25378563T>G , CM000674.1:g.25378563T>G GRCh37
NC_000012.10:g.25269830T>G NCBI36
NG_007524.1:g.30292A>C
NG_007524.2:g.30375A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15718A>C ENSP00000452512.1:n.112-15718A>C
ENST00000685328.1:c.435A>C ENSP00000508921.1:p.Ser145=
ENST00000686877.1:c.*406A>C ENSP00000510431.1:n.*406A>C
ENST00000687356.1:c.*133A>C ENSP00000510511.1:n.*133A>C
ENST00000688228.1:n.909A>C
ENST00000688940.1:c.435A>C ENSP00000509238.1:p.Ser145=
ENST00000690406.1:c.145A>C
ENST00000690804.1:c.*396A>C ENSP00000508568.1:n.*396A>C
ENST00000692768.1:c.237A>C ENSP00000510254.1:p.Ser79=
ENST00000693229.1:c.360A>C ENSP00000509223.1:p.Ser120=
ENST00000256078.10:c.435A>C MANE Plus Clinical ENSP00000256078.5:p.Ser145=
ENST00000311936.8:c.435A>C MANE Select ENSP00000308495.3:p.Ser145=
ENST00000256078.8:c.435A>C ENSP00000256078.4:p.Ser145=
ENST00000311936.7:c.435A>C ENSP00000308495.3:p.Ser145=
ENST00000557334.5:c.112-15718A>C ENSP00000452512.1:n.112-15718A>C
NM_004985.4:c.435A>C NP_004976.2:p.Ser145=
NM_033360.3:c.435A>C NP_203524.1:p.Ser145=
XM_006719069.2:c.435A>C XP_006719132.1:p.Ser145=
XM_011520653.1:c.435A>C XP_011518955.1:p.Ser145=
XM_006719069.4:c.435A>C XP_006719132.1:p.Ser145=
XM_011520653.3:c.435A>C XP_011518955.1:p.Ser145=
NM_001369786.1:c.435A>C NP_001356715.1:p.Ser145=
NM_001369787.1:c.435A>C NP_001356716.1:p.Ser145=
NM_004985.5:c.435A>C MANE Select NP_004976.2:p.Ser145=
NM_033360.4:c.435A>C MANE Plus Clinical NP_203524.1:p.Ser145=