Canonical Allele Identifier: CA2022884549

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209821_25209824delinsACTT , CM000674.2:g.25209821_25209824delinsACTT	GRCh38
NC_000012.11:g.25362755_25362758delinsACTT , CM000674.1:g.25362755_25362758delinsACTT	GRCh37
NC_000012.10:g.25254022_25254025delinsACTT	NCBI36
NG_007524.1:g.46097_46100delinsAAGT
NG_007524.2:g.46180_46183delinsAAGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.199_202delinsAAGT	ENSP00000452512.1:p.Lys67=
ENST00000685328.1:c.538_541delinsAAGT	ENSP00000508921.1:p.Lys180=
ENST00000686877.1:c.*509_*512delinsAAGT	ENSP00000510431.1:n.*509_*512delinsAAGT
ENST00000687356.1:c.*236_*239delinsAAGT	ENSP00000510511.1:n.*236_*239delinsAAGT
ENST00000688228.1:n.1012_1015delinsAAGT
ENST00000688940.1:c.538_541delinsAAGT	ENSP00000509238.1:p.Lys180=
ENST00000690406.1:c.341_344delinsAAGT
ENST00000690804.1:c.*499_*502delinsAAGT	ENSP00000508568.1:n.*499_*502delinsAAGT
ENST00000692768.1:c.340_343delinsAAGT	ENSP00000510254.1:p.Lys114=
ENST00000693229.1:c.463_466delinsAAGT	ENSP00000509223.1:p.Lys155=
ENST00000256078.10:c.*92_*95delinsAAGT MANE Plus Clinical	ENSP00000256078.5:n.*92_*95delinsAAGT
ENST00000311936.8:c.538_541delinsAAGT MANE Select	ENSP00000308495.3:p.Lys180=
ENST00000256078.8:c.*92_*95delinsAAGT	ENSP00000256078.4:n.*92_*95delinsAAGT
ENST00000311936.7:c.538_541delinsAAGT	ENSP00000308495.3:p.Lys180=
ENST00000557334.5:c.199_202delinsAAGT	ENSP00000452512.1:p.Lys67=
NM_004985.4:c.538_541delinsAAGT	NP_004976.2:p.Lys180=
NM_033360.3:c.*92_*95delinsAAGT	NP_203524.1:n.*92_*95delinsAAGT
XM_011520653.1:c.538_541delinsAAGT	XP_011518955.1:p.Lys180=
XM_011520653.3:c.538_541delinsAAGT	XP_011518955.1:p.Lys180=
NM_001369786.1:c.*92_*95delinsAAGT	NP_001356715.1:n.*92_*95delinsAAGT
NM_001369787.1:c.538_541delinsAAGT	NP_001356716.1:p.Lys180=
NM_004985.5:c.538_541delinsAAGT MANE Select	NP_004976.2:p.Lys180=
NM_033360.4:c.*92_*95delinsAAGT MANE Plus Clinical	NP_203524.1:n.*92_*95delinsAAGT