Canonical Allele Identifier: CA234211288

Gene: KRAS

Linked Data

• dbSNP Id: rs1042560787
• gnomAD v2: 12-25368252-ATCTTT-A
• gnomAD v3: 12-25215318-ATCTTT-A
• gnomAD v4: 12-25215318-ATCTTT-A
• MyVariant Identifiers: chr12:g.25368253_25368257del (hg19) ; chr12:g.25215319_25215323del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215320_25215324del , CM000674.2:g.25215320_25215324del	GRCh38
NC_000012.11:g.25368254_25368258del , CM000674.1:g.25368254_25368258del	GRCh37
NC_000012.10:g.25259521_25259525del	NCBI36
NG_007524.1:g.40598_40602del
NG_007524.2:g.40681_40685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5412_112-5408del	ENSP00000452512.1:n.112-5412_112-5408del
ENST00000685328.1:c.451-5412_451-5408del	ENSP00000508921.1:n.451-5412_451-5408del
ENST00000686877.1:c.*422-5412_*422-5408del	ENSP00000510431.1:n.*422-5412_*422-5408del
ENST00000687356.1:c.*149-5412_*149-5408del	ENSP00000510511.1:n.*149-5412_*149-5408del
ENST00000688228.1:n.925-5412_925-5408del
ENST00000688940.1:c.451-5412_451-5408del	ENSP00000509238.1:n.451-5412_451-5408del
ENST00000690406.1:c.161-2117_161-2113del
ENST00000690804.1:c.*412-5412_*412-5408del	ENSP00000508568.1:n.*412-5412_*412-5408del
ENST00000692768.1:c.253-5412_253-5408del	ENSP00000510254.1:n.253-5412_253-5408del
ENST00000693229.1:c.376-5412_376-5408del	ENSP00000509223.1:n.376-5412_376-5408del
ENST00000256078.10:c.*4+114_*4+118del MANE Plus Clinical	ENSP00000256078.5:n.*4+114_*4+118del
ENST00000311936.8:c.451-5412_451-5408del MANE Select	ENSP00000308495.3:n.451-5412_451-5408del
ENST00000256078.8:c.*4+114_*4+118del	ENSP00000256078.4:n.*4+114_*4+118del
ENST00000311936.7:c.451-5412_451-5408del	ENSP00000308495.3:n.451-5412_451-5408del
ENST00000557334.5:c.112-5412_112-5408del	ENSP00000452512.1:n.112-5412_112-5408del
NM_004985.4:c.451-5412_451-5408del	NP_004976.2:n.451-5412_451-5408del
NM_033360.3:c.*4+114_*4+118del	NP_203524.1:n.*4+114_*4+118del
XM_006719069.2:c.*4+114_*4+118del	XP_006719132.1:n.*4+114_*4+118del
XM_011520653.1:c.451-5412_451-5408del	XP_011518955.1:n.451-5412_451-5408del
XM_006719069.4:c.*4+114_*4+118del	XP_006719132.1:n.*4+114_*4+118del
XM_011520653.3:c.451-5412_451-5408del	XP_011518955.1:n.451-5412_451-5408del
NM_001369786.1:c.*4+114_*4+118del	NP_001356715.1:n.*4+114_*4+118del
NM_001369787.1:c.451-5412_451-5408del	NP_001356716.1:n.451-5412_451-5408del
NM_004985.5:c.451-5412_451-5408del MANE Select	NP_004976.2:n.451-5412_451-5408del
NM_033360.4:c.*4+114_*4+118del MANE Plus Clinical	NP_203524.1:n.*4+114_*4+118del