Canonical Allele Identifier: CA2022905802
Gene: KRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25225591G= , CM000674.2:g.25225591G= GRCh38
NC_000012.11:g.25378525G= , CM000674.1:g.25378525G= GRCh37
NC_000012.10:g.25269792G= NCBI36
NG_007524.1:g.30330C=
NG_007524.2:g.30413C=

Transcript Alleles

HGVS Amino-acid change
ENST00000256078.10:c.450+23C= ENSP00000256078.5:p.=
ENST00000311936.8:c.450+23C= MANE Select ENSP00000308495.3:p.=
ENST00000256078.8:c.450+23C= ENSP00000256078.4:p.=
ENST00000311936.7:c.450+23C= ENSP00000308495.3:p.=
ENST00000557334.5:c.112-15680C= ENSP00000452512.1:p.=
NM_004985.4:c.450+23C= NP_004976.2:p.=
NM_033360.3:c.450+23C= NP_203524.1:p.=
XM_006719069.2:c.450+23C= XP_006719132.1:p.=
XM_011520653.1:c.450+23C= XP_011518955.1:p.=
XM_006719069.4:c.450+23C= XP_006719132.1:p.=
XM_011520653.3:c.450+23C= XP_011518955.1:p.=
NM_001369786.1:c.450+23C= NP_001356715.1:p.=
NM_001369787.1:c.450+23C= NP_001356716.1:p.=
NM_004985.5:c.450+23C= MANE Select NP_004976.2:p.=
NM_033360.4:c.450+23C= NP_203524.1:p.=