Canonical Allele Identifier: CA384151125

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378573A>T (hg19) ; chr12:g.25225639A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225639A>T , CM000674.2:g.25225639A>T	GRCh38
NC_000012.11:g.25378573A>T , CM000674.1:g.25378573A>T	GRCh37
NC_000012.10:g.25269840A>T	NCBI36
NG_007524.1:g.30282T>A
NG_007524.2:g.30365T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15728T>A	ENSP00000452512.1:n.112-15728T>A
ENST00000685328.1:c.425T>A	ENSP00000508921.1:p.Ile142Asn
ENST00000686877.1:c.*396T>A	ENSP00000510431.1:n.*396T>A
ENST00000687356.1:c.*123T>A	ENSP00000510511.1:n.*123T>A
ENST00000688228.1:n.899T>A
ENST00000688940.1:c.425T>A	ENSP00000509238.1:p.Ile142Asn
ENST00000690406.1:c.135T>A
ENST00000690804.1:c.*386T>A	ENSP00000508568.1:n.*386T>A
ENST00000692768.1:c.227T>A	ENSP00000510254.1:p.Ile76Asn
ENST00000693229.1:c.350T>A	ENSP00000509223.1:p.Ile117Asn
ENST00000256078.10:c.425T>A MANE Plus Clinical	ENSP00000256078.5:p.Ile142Asn
ENST00000311936.8:c.425T>A MANE Select	ENSP00000308495.3:p.Ile142Asn
ENST00000256078.8:c.425T>A	ENSP00000256078.4:p.Ile142Asn
ENST00000311936.7:c.425T>A	ENSP00000308495.3:p.Ile142Asn
ENST00000557334.5:c.112-15728T>A	ENSP00000452512.1:n.112-15728T>A
NM_004985.4:c.425T>A	NP_004976.2:p.Ile142Asn
NM_033360.3:c.425T>A	NP_203524.1:p.Ile142Asn
XM_006719069.2:c.425T>A	XP_006719132.1:p.Ile142Asn
XM_011520653.1:c.425T>A	XP_011518955.1:p.Ile142Asn
XM_006719069.4:c.425T>A	XP_006719132.1:p.Ile142Asn
XM_011520653.3:c.425T>A	XP_011518955.1:p.Ile142Asn
NM_001369786.1:c.425T>A	NP_001356715.1:p.Ile142Asn
NM_001369787.1:c.425T>A	NP_001356716.1:p.Ile142Asn
NM_004985.5:c.425T>A MANE Select	NP_004976.2:p.Ile142Asn
NM_033360.4:c.425T>A MANE Plus Clinical	NP_203524.1:p.Ile142Asn