Canonical Allele Identifier: CA945764146

Gene: KRAS

Linked Data

• gnomAD v3: 12-25225339-AC-A
• gnomAD v4: 12-25225339-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225341del , CM000674.2:g.25225341del	GRCh38
NC_000012.11:g.25378275del , CM000674.1:g.25378275del	GRCh37
NC_000012.10:g.25269542del	NCBI36
NG_007524.1:g.30581del
NG_007524.2:g.30664del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15429del	ENSP00000452512.1:n.112-15429del
ENST00000685328.1:c.450+274del	ENSP00000508921.1:n.450+274del
ENST00000686877.1:c.*421+274del	ENSP00000510431.1:n.*421+274del
ENST00000687356.1:c.*148+274del	ENSP00000510511.1:n.*148+274del
ENST00000688228.1:n.924+274del
ENST00000688940.1:c.450+274del	ENSP00000509238.1:n.450+274del
ENST00000690406.1:c.160+274del
ENST00000690804.1:c.*411+274del	ENSP00000508568.1:n.*411+274del
ENST00000692768.1:c.252+274del	ENSP00000510254.1:n.252+274del
ENST00000693229.1:c.375+274del	ENSP00000509223.1:n.375+274del
ENST00000256078.10:c.450+274del MANE Plus Clinical	ENSP00000256078.5:n.450+274del
ENST00000311936.8:c.450+274del MANE Select	ENSP00000308495.3:n.450+274del
ENST00000256078.8:c.450+274del	ENSP00000256078.4:n.450+274del
ENST00000311936.7:c.450+274del	ENSP00000308495.3:n.450+274del
ENST00000557334.5:c.112-15429del	ENSP00000452512.1:n.112-15429del
NM_004985.4:c.450+274del	NP_004976.2:n.450+274del
NM_033360.3:c.450+274del	NP_203524.1:n.450+274del
XM_006719069.2:c.450+274del	XP_006719132.1:n.450+274del
XM_011520653.1:c.450+274del	XP_011518955.1:n.450+274del
XM_006719069.4:c.450+274del	XP_006719132.1:n.450+274del
XM_011520653.3:c.450+274del	XP_011518955.1:n.450+274del
NM_001369786.1:c.450+274del	NP_001356715.1:n.450+274del
NM_001369787.1:c.450+274del	NP_001356716.1:n.450+274del
NM_004985.5:c.450+274del MANE Select	NP_004976.2:n.450+274del
NM_033360.4:c.450+274del MANE Plus Clinical	NP_203524.1:n.450+274del