Canonical Allele Identifier: CA2022909407

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227156_25227157delinsTG , CM000674.2:g.25227156_25227157delinsTG	GRCh38
NC_000012.11:g.25380090_25380091delinsTG , CM000674.1:g.25380090_25380091delinsTG	GRCh37
NC_000012.10:g.25271357_25271358delinsTG	NCBI36
NG_007524.1:g.28764_28765delinsCA
NG_007524.2:g.28847_28848delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17246_112-17245delinsCA	ENSP00000452512.1:n.112-17246_112-17245delinsCA
ENST00000685328.1:c.290+77_290+78delinsCA	ENSP00000508921.1:n.290+77_290+78delinsCA
ENST00000686877.1:c.*261+77_*261+78delinsCA	ENSP00000510431.1:n.*261+77_*261+78delinsCA
ENST00000687356.1:c.112-1384_112-1383delinsCA	ENSP00000510511.1:n.112-1384_112-1383delinsCA
ENST00000688228.1:n.764+77_764+78delinsCA
ENST00000688940.1:c.290+77_290+78delinsCA	ENSP00000509238.1:n.290+77_290+78delinsCA
ENST00000690804.1:c.*251+77_*251+78delinsCA	ENSP00000508568.1:n.*251+77_*251+78delinsCA
ENST00000692768.1:c.92+77_92+78delinsCA	ENSP00000510254.1:n.92+77_92+78delinsCA
ENST00000693229.1:c.215+77_215+78delinsCA	ENSP00000509223.1:n.215+77_215+78delinsCA
ENST00000256078.10:c.290+77_290+78delinsCA MANE Plus Clinical	ENSP00000256078.5:n.290+77_290+78delinsCA
ENST00000311936.8:c.290+77_290+78delinsCA MANE Select	ENSP00000308495.3:n.290+77_290+78delinsCA
ENST00000256078.8:c.290+77_290+78delinsCA	ENSP00000256078.4:n.290+77_290+78delinsCA
ENST00000311936.7:c.290+77_290+78delinsCA	ENSP00000308495.3:n.290+77_290+78delinsCA
ENST00000557334.5:c.112-17246_112-17245delinsCA	ENSP00000452512.1:n.112-17246_112-17245delinsCA
NM_004985.4:c.290+77_290+78delinsCA	NP_004976.2:n.290+77_290+78delinsCA
NM_033360.3:c.290+77_290+78delinsCA	NP_203524.1:n.290+77_290+78delinsCA
XM_006719069.2:c.290+77_290+78delinsCA	XP_006719132.1:n.290+77_290+78delinsCA
XM_011520653.1:c.290+77_290+78delinsCA	XP_011518955.1:n.290+77_290+78delinsCA
XM_006719069.4:c.290+77_290+78delinsCA	XP_006719132.1:n.290+77_290+78delinsCA
XM_011520653.3:c.290+77_290+78delinsCA	XP_011518955.1:n.290+77_290+78delinsCA
NM_001369786.1:c.290+77_290+78delinsCA	NP_001356715.1:n.290+77_290+78delinsCA
NM_001369787.1:c.290+77_290+78delinsCA	NP_001356716.1:n.290+77_290+78delinsCA
NM_004985.5:c.290+77_290+78delinsCA MANE Select	NP_004976.2:n.290+77_290+78delinsCA
NM_033360.4:c.290+77_290+78delinsCA MANE Plus Clinical	NP_203524.1:n.290+77_290+78delinsCA