Canonical Allele Identifier: CA2022890335

Gene: KRAS

Linked Data

• dbSNP Id: rs1951244993
• gnomAD v4: 12-25215523-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215530_25215531del , CM000674.2:g.25215530_25215531del	GRCh38
NG_007524.2:g.40479_40480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5614_112-5613del	ENSP00000452512.1:n.112-5614_112-5613del
ENST00000685328.1:c.451-5614_451-5613del	ENSP00000508921.1:n.451-5614_451-5613del
ENST00000686877.1:c.*422-5614_*422-5613del	ENSP00000510431.1:n.*422-5614_*422-5613del
ENST00000687356.1:c.*149-5614_*149-5613del	ENSP00000510511.1:n.*149-5614_*149-5613del
ENST00000688228.1:n.925-5614_925-5613del
ENST00000688940.1:c.451-5614_451-5613del	ENSP00000509238.1:n.451-5614_451-5613del
ENST00000690406.1:c.161-2319_161-2318del
ENST00000690804.1:c.*412-5614_*412-5613del	ENSP00000508568.1:n.*412-5614_*412-5613del
ENST00000692768.1:c.253-5614_253-5613del	ENSP00000510254.1:n.253-5614_253-5613del
ENST00000693229.1:c.376-5614_376-5613del	ENSP00000509223.1:n.376-5614_376-5613del
ENST00000256078.10:c.486_487del MANE Plus Clinical	ENSP00000256078.5:p.Glu162AspfsTer22
ENST00000311936.8:c.451-5614_451-5613del MANE Select	ENSP00000308495.3:n.451-5614_451-5613del
ENST00000256078.8:c.486_487del	ENSP00000256078.4:p.Glu162AspfsTer22
ENST00000311936.7:c.451-5614_451-5613del	ENSP00000308495.3:n.451-5614_451-5613del
ENST00000557334.5:c.112-5614_112-5613del	ENSP00000452512.1:n.112-5614_112-5613del
NM_004985.4:c.451-5614_451-5613del	NP_004976.2:n.451-5614_451-5613del
XM_006719069.2:c.486_487del	XP_006719132.1:p.Glu162AspfsTer22
XM_011520653.1:c.451-5614_451-5613del	XP_011518955.1:n.451-5614_451-5613del
XM_006719069.4:c.486_487del	XP_006719132.1:p.Glu162AspfsTer22
XM_011520653.3:c.451-5614_451-5613del	XP_011518955.1:n.451-5614_451-5613del
NM_001369786.1:c.486_487del	NP_001356715.1:p.Glu162AspfsTer22
NM_001369787.1:c.451-5614_451-5613del	NP_001356716.1:n.451-5614_451-5613del
NM_004985.5:c.451-5614_451-5613del MANE Select	NP_004976.2:n.451-5614_451-5613del
NM_033360.4:c.486_487del MANE Plus Clinical	NP_203524.1:p.Glu162AspfsTer22