Canonical Allele Identifier: CA2022909485

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227185_25227186delinsAC , CM000674.2:g.25227185_25227186delinsAC	GRCh38
NC_000012.11:g.25380119_25380120delinsAC , CM000674.1:g.25380119_25380120delinsAC	GRCh37
NC_000012.10:g.25271386_25271387delinsAC	NCBI36
NG_007524.1:g.28735_28736delinsGT
NG_007524.2:g.28818_28819delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17275_112-17274delinsGT	ENSP00000452512.1:n.112-17275_112-17274de...
ENST00000685328.1:c.290+48_290+49delinsGT	ENSP00000508921.1:n.290+48_290+49delinsGT...
ENST00000686877.1:c.*261+48_*261+49delinsGT	ENSP00000510431.1:n.*261+48_*261+49delins...
ENST00000687356.1:c.112-1413_112-1412delinsGT	ENSP00000510511.1:n.112-1413_112-1412deli...
ENST00000688228.1:n.764+48_764+49delinsGT
ENST00000688940.1:c.290+48_290+49delinsGT	ENSP00000509238.1:n.290+48_290+49delinsGT...
ENST00000690804.1:c.*251+48_*251+49delinsGT	ENSP00000508568.1:n.*251+48_*251+49delins...
ENST00000692768.1:c.92+48_92+49delinsGT	ENSP00000510254.1:n.92+48_92+49delinsGT
ENST00000693229.1:c.215+48_215+49delinsGT	ENSP00000509223.1:n.215+48_215+49delinsGT...
ENST00000256078.10:c.290+48_290+49delinsGT MANE Plus Clinical	ENSP00000256078.5:n.290+48_290+49delinsGT...
ENST00000311936.8:c.290+48_290+49delinsGT MANE Select	ENSP00000308495.3:n.290+48_290+49delinsGT...
ENST00000256078.8:c.290+48_290+49delinsGT	ENSP00000256078.4:n.290+48_290+49delinsGT...
ENST00000311936.7:c.290+48_290+49delinsGT	ENSP00000308495.3:n.290+48_290+49delinsGT...
ENST00000557334.5:c.112-17275_112-17274delinsGT	ENSP00000452512.1:n.112-17275_112-17274de...
NM_004985.4:c.290+48_290+49delinsGT	NP_004976.2:n.290+48_290+49delinsGT
NM_033360.3:c.290+48_290+49delinsGT	NP_203524.1:n.290+48_290+49delinsGT
XM_006719069.2:c.290+48_290+49delinsGT	XP_006719132.1:n.290+48_290+49delinsGT
XM_011520653.1:c.290+48_290+49delinsGT	XP_011518955.1:n.290+48_290+49delinsGT
XM_006719069.4:c.290+48_290+49delinsGT	XP_006719132.1:n.290+48_290+49delinsGT
XM_011520653.3:c.290+48_290+49delinsGT	XP_011518955.1:n.290+48_290+49delinsGT
NM_001369786.1:c.290+48_290+49delinsGT	NP_001356715.1:n.290+48_290+49delinsGT
NM_001369787.1:c.290+48_290+49delinsGT	NP_001356716.1:n.290+48_290+49delinsGT
NM_004985.5:c.290+48_290+49delinsGT MANE Select	NP_004976.2:n.290+48_290+49delinsGT
NM_033360.4:c.290+48_290+49delinsGT MANE Plus Clinical	NP_203524.1:n.290+48_290+49delinsGT