Canonical Allele Identifier: CA6486894

Gene: KRAS

Linked Data

• dbSNP Id: rs775903842
• ExAC: 12:25378749 C / CTG
• gnomAD v4: 12-25225815-C-CTG
• MyVariant Identifiers: chr12:g.25378749_25378750insTG (hg19) ; chr12:g.25225815_25225816insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225815_25225816insTG , CM000674.2:g.25225815_25225816insTG	GRCh38
NC_000012.11:g.25378749_25378750insTG , CM000674.1:g.25378749_25378750insTG	GRCh37
NC_000012.10:g.25270016_25270017insTG	NCBI36
NG_007524.1:g.30105_30106insCA
NG_007524.2:g.30188_30189insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15905_112-15904insCA	ENSP00000452512.1:n.112-15905_112-15904insCA
ENST00000685328.1:c.291-43_291-42insCA	ENSP00000508921.1:n.291-43_291-42insCA
ENST00000686877.1:c.*262-43_*262-42insCA	ENSP00000510431.1:n.*262-43_*262-42insCA
ENST00000687356.1:c.112-43_112-42insCA	ENSP00000510511.1:n.112-43_112-42insCA
ENST00000688228.1:n.765-43_765-42insCA
ENST00000688940.1:c.291-43_291-42insCA	ENSP00000509238.1:n.291-43_291-42insCA
ENST00000690804.1:c.*252-43_*252-42insCA	ENSP00000508568.1:n.*252-43_*252-42insCA
ENST00000692768.1:c.93-43_93-42insCA	ENSP00000510254.1:n.93-43_93-42insCA
ENST00000693229.1:c.216-43_216-42insCA	ENSP00000509223.1:n.216-43_216-42insCA
ENST00000256078.10:c.291-43_291-42insCA MANE Plus Clinical	ENSP00000256078.5:n.291-43_291-42insCA
ENST00000311936.8:c.291-43_291-42insCA MANE Select	ENSP00000308495.3:n.291-43_291-42insCA
ENST00000256078.8:c.291-43_291-42insCA	ENSP00000256078.4:n.291-43_291-42insCA
ENST00000311936.7:c.291-43_291-42insCA	ENSP00000308495.3:n.291-43_291-42insCA
ENST00000557334.5:c.112-15905_112-15904insCA	ENSP00000452512.1:n.112-15905_112-15904insCA
NM_004985.4:c.291-43_291-42insCA	NP_004976.2:n.291-43_291-42insCA
NM_033360.3:c.291-43_291-42insCA	NP_203524.1:n.291-43_291-42insCA
XM_006719069.2:c.291-43_291-42insCA	XP_006719132.1:n.291-43_291-42insCA
XM_011520653.1:c.291-43_291-42insCA	XP_011518955.1:n.291-43_291-42insCA
XM_006719069.4:c.291-43_291-42insCA	XP_006719132.1:n.291-43_291-42insCA
XM_011520653.3:c.291-43_291-42insCA	XP_011518955.1:n.291-43_291-42insCA
NM_001369786.1:c.291-43_291-42insCA	NP_001356715.1:n.291-43_291-42insCA
NM_001369787.1:c.291-43_291-42insCA	NP_001356716.1:n.291-43_291-42insCA
NM_004985.5:c.291-43_291-42insCA MANE Select	NP_004976.2:n.291-43_291-42insCA
NM_033360.4:c.291-43_291-42insCA MANE Plus Clinical	NP_203524.1:n.291-43_291-42insCA