Canonical Allele Identifier: CA603691304

Gene: KRAS

Linked Data

• dbSNP Id: rs1344580985
• gnomAD v2: 12-25362664-TTAGTG-T
• gnomAD v3: 12-25209730-TTAGTG-T
• gnomAD v4: 12-25209730-TTAGTG-T
• MyVariant Identifiers: chr12:g.25362665_25362669del (hg19) ; chr12:g.25209731_25209735del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209733_25209737del , CM000674.2:g.25209733_25209737del	GRCh38
NC_000012.11:g.25362667_25362671del , CM000674.1:g.25362667_25362671del	GRCh37
NC_000012.10:g.25253934_25253938del	NCBI36
NG_007524.1:g.46186_46190del
NG_007524.2:g.46269_46273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*60_*64del	ENSP00000452512.1:n.*60_*64del
ENST00000685328.1:c.*60_*64del	ENSP00000508921.1:n.*60_*64del
ENST00000686877.1:c.*598_*602del	ENSP00000510431.1:n.*598_*602del
ENST00000687356.1:c.*325_*329del	ENSP00000510511.1:n.*325_*329del
ENST00000688228.1:n.1101_1105del
ENST00000688940.1:c.*60_*64del	ENSP00000509238.1:n.*60_*64del
ENST00000690406.1:c.430_434del
ENST00000690804.1:c.*588_*592del	ENSP00000508568.1:n.*588_*592del
ENST00000692768.1:c.*60_*64del	ENSP00000510254.1:n.*60_*64del
ENST00000693229.1:c.*60_*64del	ENSP00000509223.1:n.*60_*64del
ENST00000256078.10:c.*181_*185del MANE Plus Clinical	ENSP00000256078.5:n.*181_*185del
ENST00000311936.8:c.*60_*64del MANE Select	ENSP00000308495.3:n.*60_*64del
ENST00000256078.8:c.*181_*185del	ENSP00000256078.4:n.*181_*185del
ENST00000311936.7:c.*60_*64del	ENSP00000308495.3:n.*60_*64del
ENST00000557334.5:c.*60_*64del	ENSP00000452512.1:n.*60_*64del
NM_004985.4:c.*60_*64del	NP_004976.2:n.*60_*64del
NM_033360.3:c.*181_*185del	NP_203524.1:n.*181_*185del
XM_011520653.1:c.*60_*64del	XP_011518955.1:n.*60_*64del
XM_011520653.3:c.*60_*64del	XP_011518955.1:n.*60_*64del
NM_001369786.1:c.*181_*185del	NP_001356715.1:n.*181_*185del
NM_001369787.1:c.*60_*64del	NP_001356716.1:n.*60_*64del
NM_004985.5:c.*60_*64del MANE Select	NP_004976.2:n.*60_*64del
NM_033360.4:c.*181_*185del MANE Plus Clinical	NP_203524.1:n.*181_*185del