Canonical Allele Identifier: CA603968280

Gene: KRAS

Linked Data

• dbSNP Id: rs1209223906
• gnomAD v2: 12-25380056-ATTAT-A
• gnomAD v3: 12-25227122-ATTAT-A
• gnomAD v4: 12-25227122-ATTAT-A
• MyVariant Identifiers: chr12:g.25380057_25380060del (hg19) ; chr12:g.25227123_25227126del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227126_25227129del , CM000674.2:g.25227126_25227129del	GRCh38
NC_000012.11:g.25380060_25380063del , CM000674.1:g.25380060_25380063del	GRCh37
NC_000012.10:g.25271327_25271330del	NCBI36
NG_007524.1:g.28795_28798del
NG_007524.2:g.28878_28881del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-17215_112-17212del	ENSP00000452512.1:n.112-17215_112-17212del
ENST00000685328.1:c.290+108_290+111del	ENSP00000508921.1:n.290+108_290+111del
ENST00000686877.1:c.*261+108_*261+111del	ENSP00000510431.1:n.*261+108_*261+111del
ENST00000687356.1:c.112-1353_112-1350del	ENSP00000510511.1:n.112-1353_112-1350del
ENST00000688228.1:n.764+108_764+111del
ENST00000688940.1:c.290+108_290+111del	ENSP00000509238.1:n.290+108_290+111del
ENST00000690804.1:c.*251+108_*251+111del	ENSP00000508568.1:n.*251+108_*251+111del
ENST00000692768.1:c.92+108_92+111del	ENSP00000510254.1:n.92+108_92+111del
ENST00000693229.1:c.215+108_215+111del	ENSP00000509223.1:n.215+108_215+111del
ENST00000256078.10:c.290+108_290+111del MANE Plus Clinical	ENSP00000256078.5:n.290+108_290+111del
ENST00000311936.8:c.290+108_290+111del MANE Select	ENSP00000308495.3:n.290+108_290+111del
ENST00000256078.8:c.290+108_290+111del	ENSP00000256078.4:n.290+108_290+111del
ENST00000311936.7:c.290+108_290+111del	ENSP00000308495.3:n.290+108_290+111del
ENST00000557334.5:c.112-17215_112-17212del	ENSP00000452512.1:n.112-17215_112-17212del
NM_004985.4:c.290+108_290+111del	NP_004976.2:n.290+108_290+111del
NM_033360.3:c.290+108_290+111del	NP_203524.1:n.290+108_290+111del
XM_006719069.2:c.290+108_290+111del	XP_006719132.1:n.290+108_290+111del
XM_011520653.1:c.290+108_290+111del	XP_011518955.1:n.290+108_290+111del
XM_006719069.4:c.290+108_290+111del	XP_006719132.1:n.290+108_290+111del
XM_011520653.3:c.290+108_290+111del	XP_011518955.1:n.290+108_290+111del
NM_001369786.1:c.290+108_290+111del	NP_001356715.1:n.290+108_290+111del
NM_001369787.1:c.290+108_290+111del	NP_001356716.1:n.290+108_290+111del
NM_004985.5:c.290+108_290+111del MANE Select	NP_004976.2:n.290+108_290+111del
NM_033360.4:c.290+108_290+111del MANE Plus Clinical	NP_203524.1:n.290+108_290+111del