Canonical Allele Identifier: CA2529847061

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209762_25209763del , CM000674.2:g.25209762_25209763del	GRCh38
NC_000012.11:g.25362696_25362697del , CM000674.1:g.25362696_25362697del	GRCh37
NC_000012.10:g.25253963_25253964del	NCBI36
NG_007524.1:g.46158_46159del
NG_007524.2:g.46241_46242del

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*32_*33del	ENSP00000452512.1:n.*32_*33del
ENST00000685328.1:c.*32_*33del	ENSP00000508921.1:n.*32_*33del
ENST00000686877.1:c.*570_*571del	ENSP00000510431.1:n.*570_*571del
ENST00000687356.1:c.*297_*298del	ENSP00000510511.1:n.*297_*298del
ENST00000688228.1:n.1073_1074del
ENST00000688940.1:c.*32_*33del	ENSP00000509238.1:n.*32_*33del
ENST00000690406.1:c.402_403del
ENST00000690804.1:c.*560_*561del	ENSP00000508568.1:n.*560_*561del
ENST00000692768.1:c.*32_*33del	ENSP00000510254.1:n.*32_*33del
ENST00000693229.1:c.*32_*33del	ENSP00000509223.1:n.*32_*33del
ENST00000256078.10:c.*153_*154del MANE Plus Clinical	ENSP00000256078.5:n.*153_*154del
ENST00000311936.8:c.*32_*33del MANE Select	ENSP00000308495.3:n.*32_*33del
ENST00000256078.8:c.*153_*154del	ENSP00000256078.4:n.*153_*154del
ENST00000311936.7:c.*32_*33del	ENSP00000308495.3:n.*32_*33del
ENST00000557334.5:c.*32_*33del	ENSP00000452512.1:n.*32_*33del
NM_004985.4:c.*32_*33del	NP_004976.2:n.*32_*33del
NM_033360.3:c.*153_*154del	NP_203524.1:n.*153_*154del
XM_011520653.1:c.*32_*33del	XP_011518955.1:n.*32_*33del
XM_011520653.3:c.*32_*33del	XP_011518955.1:n.*32_*33del
NM_001369786.1:c.*153_*154del	NP_001356715.1:n.*153_*154del
NM_001369787.1:c.*32_*33del	NP_001356716.1:n.*32_*33del
NM_004985.5:c.*32_*33del MANE Select	NP_004976.2:n.*32_*33del
NM_033360.4:c.*153_*154del MANE Plus Clinical	NP_203524.1:n.*153_*154del