Canonical Allele Identifier: CA2617996690

Gene: KRAS

Linked Data

• gnomAD v4: 12-25215565-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215565_25215566insAG , CM000674.2:g.25215565_25215566insAG	GRCh38
NC_000012.11:g.25368499_25368500insAG , CM000674.1:g.25368499_25368500insAG	GRCh37
NC_000012.10:g.25259766_25259767insAG	NCBI36
NG_007524.1:g.40355_40356insCT
NG_007524.2:g.40438_40439insCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-5655_112-5654insCT	ENSP00000452512.1:n.112-5655_112-5654insCT
ENST00000685328.1:c.451-5655_451-5654insCT	ENSP00000508921.1:n.451-5655_451-5654insCT
ENST00000686877.1:c.*422-5655_*422-5654insCT	ENSP00000510431.1:n.*422-5655_*422-5654insCT
ENST00000687356.1:c.*149-5655_*149-5654insCT	ENSP00000510511.1:n.*149-5655_*149-5654insCT
ENST00000688228.1:n.925-5655_925-5654insCT
ENST00000688940.1:c.451-5655_451-5654insCT	ENSP00000509238.1:n.451-5655_451-5654insCT
ENST00000690406.1:c.161-2360_161-2359insCT
ENST00000690804.1:c.*412-5655_*412-5654insCT	ENSP00000508568.1:n.*412-5655_*412-5654insCT
ENST00000692768.1:c.253-5655_253-5654insCT	ENSP00000510254.1:n.253-5655_253-5654insCT
ENST00000693229.1:c.376-5655_376-5654insCT	ENSP00000509223.1:n.376-5655_376-5654insCT
ENST00000256078.10:c.451-6_451-5insCT MANE Plus Clinical	ENSP00000256078.5:n.451-6_451-5insCT
ENST00000311936.8:c.451-5655_451-5654insCT MANE Select	ENSP00000308495.3:n.451-5655_451-5654insCT
ENST00000256078.8:c.451-6_451-5insCT	ENSP00000256078.4:n.451-6_451-5insCT
ENST00000311936.7:c.451-5655_451-5654insCT	ENSP00000308495.3:n.451-5655_451-5654insCT
ENST00000557334.5:c.112-5655_112-5654insCT	ENSP00000452512.1:n.112-5655_112-5654insCT
NM_004985.4:c.451-5655_451-5654insCT	NP_004976.2:n.451-5655_451-5654insCT
NM_033360.3:c.451-6_451-5insCT	NP_203524.1:n.451-6_451-5insCT
XM_006719069.2:c.451-6_451-5insCT	XP_006719132.1:n.451-6_451-5insCT
XM_011520653.1:c.451-5655_451-5654insCT	XP_011518955.1:n.451-5655_451-5654insCT
XM_006719069.4:c.451-6_451-5insCT	XP_006719132.1:n.451-6_451-5insCT
XM_011520653.3:c.451-5655_451-5654insCT	XP_011518955.1:n.451-5655_451-5654insCT
NM_001369786.1:c.451-6_451-5insCT	NP_001356715.1:n.451-6_451-5insCT
NM_001369787.1:c.451-5655_451-5654insCT	NP_001356716.1:n.451-5655_451-5654insCT
NM_004985.5:c.451-5655_451-5654insCT MANE Select	NP_004976.2:n.451-5655_451-5654insCT
NM_033360.4:c.451-6_451-5insCT MANE Plus Clinical	NP_203524.1:n.451-6_451-5insCT