Canonical Allele Identifier: CA384151536

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378670G>T (hg19) ; chr12:g.25225736G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225736G>T , CM000674.2:g.25225736G>T	GRCh38
NC_000012.11:g.25378670G>T , CM000674.1:g.25378670G>T	GRCh37
NC_000012.10:g.25269937G>T	NCBI36
NG_007524.1:g.30185C>A
NG_007524.2:g.30268C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15825C>A	ENSP00000452512.1:n.112-15825C>A
ENST00000685328.1:c.328C>A	ENSP00000508921.1:p.Pro110Thr
ENST00000686877.1:c.*299C>A	ENSP00000510431.1:n.*299C>A
ENST00000687356.1:c.*26C>A	ENSP00000510511.1:n.*26C>A
ENST00000688228.1:n.802C>A
ENST00000688940.1:c.328C>A	ENSP00000509238.1:p.Pro110Thr
ENST00000690406.1:c.38C>A
ENST00000690804.1:c.*289C>A	ENSP00000508568.1:n.*289C>A
ENST00000692768.1:c.130C>A	ENSP00000510254.1:p.Pro44Thr
ENST00000693229.1:c.253C>A	ENSP00000509223.1:p.Pro85Thr
ENST00000256078.10:c.328C>A MANE Plus Clinical	ENSP00000256078.5:p.Pro110Thr
ENST00000311936.8:c.328C>A MANE Select	ENSP00000308495.3:p.Pro110Thr
ENST00000256078.8:c.328C>A	ENSP00000256078.4:p.Pro110Thr
ENST00000311936.7:c.328C>A	ENSP00000308495.3:p.Pro110Thr
ENST00000557334.5:c.112-15825C>A	ENSP00000452512.1:n.112-15825C>A
NM_004985.4:c.328C>A	NP_004976.2:p.Pro110Thr
NM_033360.3:c.328C>A	NP_203524.1:p.Pro110Thr
XM_006719069.2:c.328C>A	XP_006719132.1:p.Pro110Thr
XM_011520653.1:c.328C>A	XP_011518955.1:p.Pro110Thr
XM_006719069.4:c.328C>A	XP_006719132.1:p.Pro110Thr
XM_011520653.3:c.328C>A	XP_011518955.1:p.Pro110Thr
NM_001369786.1:c.328C>A	NP_001356715.1:p.Pro110Thr
NM_001369787.1:c.328C>A	NP_001356716.1:p.Pro110Thr
NM_004985.5:c.328C>A MANE Select	NP_004976.2:p.Pro110Thr
NM_033360.4:c.328C>A MANE Plus Clinical	NP_203524.1:p.Pro110Thr