Canonical Allele Identifier: CA234207273

Gene: KRAS

Linked Data

• dbSNP Id: rs148135322
• gnomAD v2: 12-25363184-A-ATG
• gnomAD v3: 12-25210250-A-ATG
• gnomAD v4: 12-25210250-A-ATG
• MyVariant Identifiers: chr12:g.25363188_25363189insTG (hg19) ; chr12:g.25363184_25363185insTG (hg19) ; chr12:g.25210254_25210255insTG (hg38) ; chr12:g.25210250_25210251insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25210262_25210263dup , CM000674.2:g.25210262_25210263dup	GRCh38
NC_000012.11:g.25363196_25363197dup , CM000674.1:g.25363196_25363197dup	GRCh37
NC_000012.10:g.25254463_25254464dup	NCBI36
NG_007524.1:g.45669_45670dup
NG_007524.2:g.45752_45753dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-341_112-340dup	ENSP00000452512.1:n.112-341_112-340dup
ENST00000685328.1:c.451-341_451-340dup	ENSP00000508921.1:n.451-341_451-340dup
ENST00000686877.1:c.*422-341_*422-340dup	ENSP00000510431.1:n.*422-341_*422-340dup
ENST00000687356.1:c.*149-341_*149-340dup	ENSP00000510511.1:n.*149-341_*149-340dup
ENST00000688228.1:n.925-341_925-340dup
ENST00000688940.1:c.451-341_451-340dup	ENSP00000509238.1:n.451-341_451-340dup
ENST00000690406.1:c.254-341_254-340dup
ENST00000690804.1:c.*412-341_*412-340dup	ENSP00000508568.1:n.*412-341_*412-340dup
ENST00000692768.1:c.253-341_253-340dup	ENSP00000510254.1:n.253-341_253-340dup
ENST00000693229.1:c.376-341_376-340dup	ENSP00000509223.1:n.376-341_376-340dup
ENST00000256078.10:c.*5-341_*5-340dup MANE Plus Clinical	ENSP00000256078.5:n.*5-341_*5-340dup
ENST00000311936.8:c.451-341_451-340dup MANE Select	ENSP00000308495.3:n.451-341_451-340dup
ENST00000256078.8:c.*5-341_*5-340dup	ENSP00000256078.4:n.*5-341_*5-340dup
ENST00000311936.7:c.451-341_451-340dup	ENSP00000308495.3:n.451-341_451-340dup
ENST00000557334.5:c.112-341_112-340dup	ENSP00000452512.1:n.112-341_112-340dup
NM_004985.4:c.451-341_451-340dup	NP_004976.2:n.451-341_451-340dup
NM_033360.3:c.*5-341_*5-340dup	NP_203524.1:n.*5-341_*5-340dup
XM_006719069.2:c.*5-341_*5-340dup	XP_006719132.1:n.*5-341_*5-340dup
XM_011520653.1:c.451-341_451-340dup	XP_011518955.1:n.451-341_451-340dup
XM_006719069.4:c.*5-341_*5-340dup	XP_006719132.1:n.*5-341_*5-340dup
XM_011520653.3:c.451-341_451-340dup	XP_011518955.1:n.451-341_451-340dup
NM_001369786.1:c.*5-341_*5-340dup	NP_001356715.1:n.*5-341_*5-340dup
NM_001369787.1:c.451-341_451-340dup	NP_001356716.1:n.451-341_451-340dup
NM_004985.5:c.451-341_451-340dup MANE Select	NP_004976.2:n.451-341_451-340dup
NM_033360.4:c.*5-341_*5-340dup MANE Plus Clinical	NP_203524.1:n.*5-341_*5-340dup