Canonical Allele Identifier: CA2617996360

Gene: KRAS

Linked Data

• gnomAD v4: 12-25215293-TACTAATTATGGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215296_25215308del , CM000674.2:g.25215296_25215308del	GRCh38
NC_000012.11:g.25368230_25368242del , CM000674.1:g.25368230_25368242del	GRCh37
NC_000012.10:g.25259497_25259509del	NCBI36
NG_007524.1:g.40615_40627del
NG_007524.2:g.40698_40710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5395_112-5383del	ENSP00000452512.1:n.112-5395_112-5383del
ENST00000685328.1:c.451-5395_451-5383del	ENSP00000508921.1:n.451-5395_451-5383del
ENST00000686877.1:c.*422-5395_*422-5383del	ENSP00000510431.1:n.*422-5395_*422-5383del
ENST00000687356.1:c.*149-5395_*149-5383del	ENSP00000510511.1:n.*149-5395_*149-5383del
ENST00000688228.1:n.925-5395_925-5383del
ENST00000688940.1:c.451-5395_451-5383del	ENSP00000509238.1:n.451-5395_451-5383del
ENST00000690406.1:c.161-2100_161-2088del
ENST00000690804.1:c.*412-5395_*412-5383del	ENSP00000508568.1:n.*412-5395_*412-5383del
ENST00000692768.1:c.253-5395_253-5383del	ENSP00000510254.1:n.253-5395_253-5383del
ENST00000693229.1:c.376-5395_376-5383del	ENSP00000509223.1:n.376-5395_376-5383del
ENST00000256078.10:c.*4+131_*4+143del MANE Plus Clinical	ENSP00000256078.5:n.*4+131_*4+143del
ENST00000311936.8:c.451-5395_451-5383del MANE Select	ENSP00000308495.3:n.451-5395_451-5383del
ENST00000256078.8:c.*4+131_*4+143del	ENSP00000256078.4:n.*4+131_*4+143del
ENST00000311936.7:c.451-5395_451-5383del	ENSP00000308495.3:n.451-5395_451-5383del
ENST00000557334.5:c.112-5395_112-5383del	ENSP00000452512.1:n.112-5395_112-5383del
NM_004985.4:c.451-5395_451-5383del	NP_004976.2:n.451-5395_451-5383del
NM_033360.3:c.*4+131_*4+143del	NP_203524.1:n.*4+131_*4+143del
XM_006719069.2:c.*4+131_*4+143del	XP_006719132.1:n.*4+131_*4+143del
XM_011520653.1:c.451-5395_451-5383del	XP_011518955.1:n.451-5395_451-5383del
XM_006719069.4:c.*4+131_*4+143del	XP_006719132.1:n.*4+131_*4+143del
XM_011520653.3:c.451-5395_451-5383del	XP_011518955.1:n.451-5395_451-5383del
NM_001369786.1:c.*4+131_*4+143del	NP_001356715.1:n.*4+131_*4+143del
NM_001369787.1:c.451-5395_451-5383del	NP_001356716.1:n.451-5395_451-5383del
NM_004985.5:c.451-5395_451-5383del MANE Select	NP_004976.2:n.451-5395_451-5383del
NM_033360.4:c.*4+131_*4+143del MANE Plus Clinical	NP_203524.1:n.*4+131_*4+143del