Canonical Allele Identifier: CA2617994357

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209775-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209781dup , CM000674.2:g.25209781dup	GRCh38
NC_000012.11:g.25362715dup , CM000674.1:g.25362715dup	GRCh37
NC_000012.10:g.25253982dup	NCBI36
NG_007524.1:g.46145dup
NG_007524.2:g.46228dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*19dup	ENSP00000452512.1:n.*19dup
ENST00000685328.1:c.*19dup	ENSP00000508921.1:n.*19dup
ENST00000686877.1:c.*557dup	ENSP00000510431.1:n.*557dup
ENST00000687356.1:c.*284dup	ENSP00000510511.1:n.*284dup
ENST00000688228.1:n.1060dup
ENST00000688940.1:c.*19dup	ENSP00000509238.1:n.*19dup
ENST00000690406.1:c.389dup
ENST00000690804.1:c.*547dup	ENSP00000508568.1:n.*547dup
ENST00000692768.1:c.*19dup	ENSP00000510254.1:n.*19dup
ENST00000693229.1:c.*19dup	ENSP00000509223.1:n.*19dup
ENST00000256078.10:c.*140dup MANE Plus Clinical	ENSP00000256078.5:n.*140dup
ENST00000311936.8:c.*19dup MANE Select	ENSP00000308495.3:n.*19dup
ENST00000256078.8:c.*140dup	ENSP00000256078.4:n.*140dup
ENST00000311936.7:c.*19dup	ENSP00000308495.3:n.*19dup
ENST00000557334.5:c.*19dup	ENSP00000452512.1:n.*19dup
NM_004985.4:c.*19dup	NP_004976.2:n.*19dup
NM_033360.3:c.*140dup	NP_203524.1:n.*140dup
XM_011520653.1:c.*19dup	XP_011518955.1:n.*19dup
XM_011520653.3:c.*19dup	XP_011518955.1:n.*19dup
NM_001369786.1:c.*140dup	NP_001356715.1:n.*140dup
NM_001369787.1:c.*19dup	NP_001356716.1:n.*19dup
NM_004985.5:c.*19dup MANE Select	NP_004976.2:n.*19dup
NM_033360.4:c.*140dup MANE Plus Clinical	NP_203524.1:n.*140dup