Canonical Allele Identifier: CA2542147048

Gene: KRAS

Linked Data

• gnomAD v4: 12-25215659-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215671_25215672dup , CM000674.2:g.25215671_25215672dup	GRCh38
NC_000012.11:g.25368605_25368606dup , CM000674.1:g.25368605_25368606dup	GRCh37
NC_000012.10:g.25259872_25259873dup	NCBI36
NG_007524.1:g.40260_40261dup
NG_007524.2:g.40343_40344dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5750_112-5749dup	ENSP00000452512.1:n.112-5750_112-5749dup
ENST00000685328.1:c.451-5750_451-5749dup	ENSP00000508921.1:n.451-5750_451-5749dup
ENST00000686877.1:c.*422-5750_*422-5749dup	ENSP00000510431.1:n.*422-5750_*422-5749dup
ENST00000687356.1:c.*149-5750_*149-5749dup	ENSP00000510511.1:n.*149-5750_*149-5749dup
ENST00000688228.1:n.925-5750_925-5749dup
ENST00000688940.1:c.451-5750_451-5749dup	ENSP00000509238.1:n.451-5750_451-5749dup
ENST00000690406.1:c.161-2455_161-2454dup
ENST00000690804.1:c.*412-5750_*412-5749dup	ENSP00000508568.1:n.*412-5750_*412-5749dup
ENST00000692768.1:c.253-5750_253-5749dup	ENSP00000510254.1:n.253-5750_253-5749dup
ENST00000693229.1:c.376-5750_376-5749dup	ENSP00000509223.1:n.376-5750_376-5749dup
ENST00000256078.10:c.451-101_451-100dup MANE Plus Clinical	ENSP00000256078.5:n.451-101_451-100dup
ENST00000311936.8:c.451-5750_451-5749dup MANE Select	ENSP00000308495.3:n.451-5750_451-5749dup
ENST00000256078.8:c.451-101_451-100dup	ENSP00000256078.4:n.451-101_451-100dup
ENST00000311936.7:c.451-5750_451-5749dup	ENSP00000308495.3:n.451-5750_451-5749dup
ENST00000557334.5:c.112-5750_112-5749dup	ENSP00000452512.1:n.112-5750_112-5749dup
NM_004985.4:c.451-5750_451-5749dup	NP_004976.2:n.451-5750_451-5749dup
NM_033360.3:c.451-101_451-100dup	NP_203524.1:n.451-101_451-100dup
XM_006719069.2:c.451-101_451-100dup	XP_006719132.1:n.451-101_451-100dup
XM_011520653.1:c.451-5750_451-5749dup	XP_011518955.1:n.451-5750_451-5749dup
XM_006719069.4:c.451-101_451-100dup	XP_006719132.1:n.451-101_451-100dup
XM_011520653.3:c.451-5750_451-5749dup	XP_011518955.1:n.451-5750_451-5749dup
NM_001369786.1:c.451-101_451-100dup	NP_001356715.1:n.451-101_451-100dup
NM_001369787.1:c.451-5750_451-5749dup	NP_001356716.1:n.451-5750_451-5749dup
NM_004985.5:c.451-5750_451-5749dup MANE Select	NP_004976.2:n.451-5750_451-5749dup
NM_033360.4:c.451-101_451-100dup MANE Plus Clinical	NP_203524.1:n.451-101_451-100dup