Canonical Allele Identifier: CA234219629

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1677688
• ClinVar RCV Id: RCV002224430
• dbSNP Id: rs373500216
• gnomAD v4: 12-25225663-G-C
• MyVariant Identifiers: chr12:g.25378597G>C (hg19) ; chr12:g.25225663G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225663G>C , CM000674.2:g.25225663G>C	GRCh38
NC_000012.11:g.25378597G>C , CM000674.1:g.25378597G>C	GRCh37
NC_000012.10:g.25269864G>C	NCBI36
NG_007524.1:g.30258C>G
NG_007524.2:g.30341C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15752C>G	ENSP00000452512.1:n.112-15752C>G
ENST00000685328.1:c.401C>G	ENSP00000508921.1:p.Ala134Gly
ENST00000686877.1:c.*372C>G	ENSP00000510431.1:n.*372C>G
ENST00000687356.1:c.*99C>G	ENSP00000510511.1:n.*99C>G
ENST00000688228.1:n.875C>G
ENST00000688940.1:c.401C>G	ENSP00000509238.1:p.Ala134Gly
ENST00000690406.1:c.111C>G
ENST00000690804.1:c.*362C>G	ENSP00000508568.1:n.*362C>G
ENST00000692768.1:c.203C>G	ENSP00000510254.1:p.Ala68Gly
ENST00000693229.1:c.326C>G	ENSP00000509223.1:p.Ala109Gly
ENST00000256078.10:c.401C>G MANE Plus Clinical	ENSP00000256078.5:p.Ala134Gly
ENST00000311936.8:c.401C>G MANE Select	ENSP00000308495.3:p.Ala134Gly
ENST00000256078.8:c.401C>G	ENSP00000256078.4:p.Ala134Gly
ENST00000311936.7:c.401C>G	ENSP00000308495.3:p.Ala134Gly
ENST00000557334.5:c.112-15752C>G	ENSP00000452512.1:n.112-15752C>G
NM_004985.4:c.401C>G	NP_004976.2:p.Ala134Gly
NM_033360.3:c.401C>G	NP_203524.1:p.Ala134Gly
XM_006719069.2:c.401C>G	XP_006719132.1:p.Ala134Gly
XM_011520653.1:c.401C>G	XP_011518955.1:p.Ala134Gly
XM_006719069.4:c.401C>G	XP_006719132.1:p.Ala134Gly
XM_011520653.3:c.401C>G	XP_011518955.1:p.Ala134Gly
NM_001369786.1:c.401C>G	NP_001356715.1:p.Ala134Gly
NM_001369787.1:c.401C>G	NP_001356716.1:p.Ala134Gly
NM_004985.5:c.401C>G MANE Select	NP_004976.2:p.Ala134Gly
NM_033360.4:c.401C>G MANE Plus Clinical	NP_203524.1:p.Ala134Gly