Canonical Allele Identifier: CA2022909635

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227262_25227263delinsTA , CM000674.2:g.25227262_25227263delinsTA	GRCh38
NC_000012.11:g.25380196_25380197delinsTA , CM000674.1:g.25380196_25380197delinsTA	GRCh37
NC_000012.10:g.25271463_25271464delinsTA	NCBI36
NG_007524.1:g.28658_28659delinsTA
NG_007524.2:g.28741_28742delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17352_112-17351delinsTA	ENSP00000452512.1:n.112-17352_112-17351delinsTA
ENST00000685328.1:c.261_262delinsTA	ENSP00000508921.1:p.Thr87=
ENST00000686877.1:c.*232_*233delinsTA	ENSP00000510431.1:n.*232_*233delinsTA
ENST00000687356.1:c.112-1490_112-1489delinsTA	ENSP00000510511.1:n.112-1490_112-1489delinsTA
ENST00000688228.1:n.735_736delinsTA
ENST00000688940.1:c.261_262delinsTA	ENSP00000509238.1:p.Thr87=
ENST00000690804.1:c.*222_*223delinsTA	ENSP00000508568.1:n.*222_*223delinsTA
ENST00000692768.1:c.63_64delinsTA	ENSP00000510254.1:p.Thr21=
ENST00000693229.1:c.186_187delinsTA	ENSP00000509223.1:p.Thr62=
ENST00000256078.10:c.261_262delinsTA MANE Plus Clinical	ENSP00000256078.5:p.Thr87=
ENST00000311936.8:c.261_262delinsTA MANE Select	ENSP00000308495.3:p.Thr87=
ENST00000256078.8:c.261_262delinsTA	ENSP00000256078.4:p.Thr87=
ENST00000311936.7:c.261_262delinsTA	ENSP00000308495.3:p.Thr87=
ENST00000557334.5:c.112-17352_112-17351delinsTA	ENSP00000452512.1:n.112-17352_112-17351delinsTA
NM_004985.4:c.261_262delinsTA	NP_004976.2:p.Thr87=
NM_033360.3:c.261_262delinsTA	NP_203524.1:p.Thr87=
XM_006719069.2:c.261_262delinsTA	XP_006719132.1:p.Thr87=
XM_011520653.1:c.261_262delinsTA	XP_011518955.1:p.Thr87=
XM_006719069.4:c.261_262delinsTA	XP_006719132.1:p.Thr87=
XM_011520653.3:c.261_262delinsTA	XP_011518955.1:p.Thr87=
NM_001369786.1:c.261_262delinsTA	NP_001356715.1:p.Thr87=
NM_001369787.1:c.261_262delinsTA	NP_001356716.1:p.Thr87=
NM_004985.5:c.261_262delinsTA MANE Select	NP_004976.2:p.Thr87=
NM_033360.4:c.261_262delinsTA MANE Plus Clinical	NP_203524.1:p.Thr87=