Canonical Allele Identifier: CA2831703308

Gene: KRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25215350C>T , CM000674.2:g.25215350C>T	GRCh38
NC_000012.11:g.25368284C>T , CM000674.1:g.25368284C>T	GRCh37
NC_000012.10:g.25259551C>T	NCBI36
NG_007524.1:g.40571G>A
NG_007524.2:g.40654G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-5439G>A	ENSP00000452512.1:n.112-5439G>A
ENST00000685328.1:c.451-5439G>A	ENSP00000508921.1:n.451-5439G>A
ENST00000686877.1:c.*422-5439G>A	ENSP00000510431.1:n.*422-5439G>A
ENST00000687356.1:c.*149-5439G>A	ENSP00000510511.1:n.*149-5439G>A
ENST00000688228.1:n.925-5439G>A
ENST00000688940.1:c.451-5439G>A	ENSP00000509238.1:n.451-5439G>A
ENST00000690406.1:c.161-2144G>A
ENST00000690804.1:c.*412-5439G>A	ENSP00000508568.1:n.*412-5439G>A
ENST00000692768.1:c.253-5439G>A	ENSP00000510254.1:n.253-5439G>A
ENST00000693229.1:c.376-5439G>A	ENSP00000509223.1:n.376-5439G>A
ENST00000256078.10:c.*4+87G>A MANE Plus Clinical	ENSP00000256078.5:n.*4+87G>A
ENST00000311936.8:c.451-5439G>A MANE Select	ENSP00000308495.3:n.451-5439G>A
ENST00000256078.8:c.*4+87G>A	ENSP00000256078.4:n.*4+87G>A
ENST00000311936.7:c.451-5439G>A	ENSP00000308495.3:n.451-5439G>A
ENST00000557334.5:c.112-5439G>A	ENSP00000452512.1:n.112-5439G>A
NM_004985.4:c.451-5439G>A	NP_004976.2:n.451-5439G>A
NM_033360.3:c.*4+87G>A	NP_203524.1:n.*4+87G>A
XM_006719069.2:c.*4+87G>A	XP_006719132.1:n.*4+87G>A
XM_011520653.1:c.451-5439G>A	XP_011518955.1:n.451-5439G>A
XM_006719069.4:c.*4+87G>A	XP_006719132.1:n.*4+87G>A
XM_011520653.3:c.451-5439G>A	XP_011518955.1:n.451-5439G>A
NM_001369786.1:c.*4+87G>A	NP_001356715.1:n.*4+87G>A
NM_001369787.1:c.451-5439G>A	NP_001356716.1:n.451-5439G>A
NM_004985.5:c.451-5439G>A MANE Select	NP_004976.2:n.451-5439G>A
NM_033360.4:c.*4+87G>A MANE Plus Clinical	NP_203524.1:n.*4+87G>A