Canonical Allele Identifier: CA2022905680
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225535A= , CM000674.2:g.25225535A= GRCh38
NC_000012.11:g.25378469A= , CM000674.1:g.25378469A= GRCh37
NC_000012.10:g.25269736A= NCBI36
NG_007524.1:g.30386T=
NG_007524.2:g.30469T=

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15624T= ENSP00000452512.1:n.112-15624T=
ENST00000685328.1:c.450+79T= ENSP00000508921.1:n.450+79T=
ENST00000686877.1:c.*421+79T= ENSP00000510431.1:n.*421+79T=
ENST00000687356.1:c.*148+79T= ENSP00000510511.1:n.*148+79T=
ENST00000688228.1:n.924+79T=
ENST00000688940.1:c.450+79T= ENSP00000509238.1:n.450+79T=
ENST00000690406.1:c.160+79T=
ENST00000690804.1:c.*411+79T= ENSP00000508568.1:n.*411+79T=
ENST00000692768.1:c.252+79T= ENSP00000510254.1:n.252+79T=
ENST00000693229.1:c.375+79T= ENSP00000509223.1:n.375+79T=
ENST00000256078.10:c.450+79T= MANE Plus Clinical ENSP00000256078.5:n.450+79T=
ENST00000311936.8:c.450+79T= MANE Select ENSP00000308495.3:n.450+79T=
ENST00000256078.8:c.450+79T= ENSP00000256078.4:n.450+79T=
ENST00000311936.7:c.450+79T= ENSP00000308495.3:n.450+79T=
ENST00000557334.5:c.112-15624T= ENSP00000452512.1:n.112-15624T=
NM_004985.4:c.450+79T= NP_004976.2:n.450+79T=
NM_033360.3:c.450+79T= NP_203524.1:n.450+79T=
XM_006719069.2:c.450+79T= XP_006719132.1:n.450+79T=
XM_011520653.1:c.450+79T= XP_011518955.1:n.450+79T=
XM_006719069.4:c.450+79T= XP_006719132.1:n.450+79T=
XM_011520653.3:c.450+79T= XP_011518955.1:n.450+79T=
NM_001369786.1:c.450+79T= NP_001356715.1:n.450+79T=
NM_001369787.1:c.450+79T= NP_001356716.1:n.450+79T=
NM_004985.5:c.450+79T= MANE Select NP_004976.2:n.450+79T=
NM_033360.4:c.450+79T= MANE Plus Clinical NP_203524.1:n.450+79T=