Canonical Allele Identifier: CA2617996583

Gene: KRAS

Linked Data

• gnomAD v4: 12-25215483-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215486_25215487del , CM000674.2:g.25215486_25215487del	GRCh38
NC_000012.11:g.25368420_25368421del , CM000674.1:g.25368420_25368421del	GRCh37
NC_000012.10:g.25259687_25259688del	NCBI36
NG_007524.1:g.40436_40437del
NG_007524.2:g.40519_40520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5574_112-5573del	ENSP00000452512.1:n.112-5574_112-5573del
ENST00000685328.1:c.451-5574_451-5573del	ENSP00000508921.1:n.451-5574_451-5573del
ENST00000686877.1:c.*422-5574_*422-5573del	ENSP00000510431.1:n.*422-5574_*422-5573del
ENST00000687356.1:c.*149-5574_*149-5573del	ENSP00000510511.1:n.*149-5574_*149-5573del
ENST00000688228.1:n.925-5574_925-5573del
ENST00000688940.1:c.451-5574_451-5573del	ENSP00000509238.1:n.451-5574_451-5573del
ENST00000690406.1:c.161-2279_161-2278del
ENST00000690804.1:c.*412-5574_*412-5573del	ENSP00000508568.1:n.*412-5574_*412-5573del
ENST00000692768.1:c.253-5574_253-5573del	ENSP00000510254.1:n.253-5574_253-5573del
ENST00000693229.1:c.376-5574_376-5573del	ENSP00000509223.1:n.376-5574_376-5573del
ENST00000256078.10:c.526_527del MANE Plus Clinical	ENSP00000256078.5:p.Lys176AspfsTer8
ENST00000311936.8:c.451-5574_451-5573del MANE Select	ENSP00000308495.3:n.451-5574_451-5573del
ENST00000256078.8:c.526_527del	ENSP00000256078.4:p.Lys176AspfsTer8
ENST00000311936.7:c.451-5574_451-5573del	ENSP00000308495.3:n.451-5574_451-5573del
ENST00000557334.5:c.112-5574_112-5573del	ENSP00000452512.1:n.112-5574_112-5573del
NM_004985.4:c.451-5574_451-5573del	NP_004976.2:n.451-5574_451-5573del
NM_033360.3:c.526_527del	NP_203524.1:p.Lys176AspfsTer8
XM_006719069.2:c.526_527del	XP_006719132.1:p.Lys176AspfsTer8
XM_011520653.1:c.451-5574_451-5573del	XP_011518955.1:n.451-5574_451-5573del
XM_006719069.4:c.526_527del	XP_006719132.1:p.Lys176AspfsTer8
XM_011520653.3:c.451-5574_451-5573del	XP_011518955.1:n.451-5574_451-5573del
NM_001369786.1:c.526_527del	NP_001356715.1:p.Lys176AspfsTer8
NM_001369787.1:c.451-5574_451-5573del	NP_001356716.1:n.451-5574_451-5573del
NM_004985.5:c.451-5574_451-5573del MANE Select	NP_004976.2:n.451-5574_451-5573del
NM_033360.4:c.526_527del MANE Plus Clinical	NP_203524.1:p.Lys176AspfsTer8