Canonical Allele Identifier: CA478890051

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378635A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225701A>C , CM000674.2:g.25225701A>C	GRCh38
NC_000012.11:g.25378635A>C , CM000674.1:g.25378635A>C	GRCh37
NC_000012.10:g.25269902A>C	NCBI36
NG_007524.1:g.30220T>G
NG_007524.2:g.30303T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15790T>G	ENSP00000452512.1:n.112-15790T>G
ENST00000685328.1:c.363T>G	ENSP00000508921.1:p.Pro121=
ENST00000686877.1:c.*334T>G	ENSP00000510431.1:n.*334T>G
ENST00000687356.1:c.*61T>G	ENSP00000510511.1:n.*61T>G
ENST00000688228.1:n.837T>G
ENST00000688940.1:c.363T>G	ENSP00000509238.1:p.Pro121=
ENST00000690406.1:c.73T>G
ENST00000690804.1:c.*324T>G	ENSP00000508568.1:n.*324T>G
ENST00000692768.1:c.165T>G	ENSP00000510254.1:p.Pro55=
ENST00000693229.1:c.288T>G	ENSP00000509223.1:p.Pro96=
ENST00000256078.10:c.363T>G MANE Plus Clinical	ENSP00000256078.5:p.Pro121=
ENST00000311936.8:c.363T>G MANE Select	ENSP00000308495.3:p.Pro121=
ENST00000256078.8:c.363T>G	ENSP00000256078.4:p.Pro121=
ENST00000311936.7:c.363T>G	ENSP00000308495.3:p.Pro121=
ENST00000557334.5:c.112-15790T>G	ENSP00000452512.1:n.112-15790T>G
NM_004985.4:c.363T>G	NP_004976.2:p.Pro121=
NM_033360.3:c.363T>G	NP_203524.1:p.Pro121=
XM_006719069.2:c.363T>G	XP_006719132.1:p.Pro121=
XM_011520653.1:c.363T>G	XP_011518955.1:p.Pro121=
XM_006719069.4:c.363T>G	XP_006719132.1:p.Pro121=
XM_011520653.3:c.363T>G	XP_011518955.1:p.Pro121=
NM_001369786.1:c.363T>G	NP_001356715.1:p.Pro121=
NM_001369787.1:c.363T>G	NP_001356716.1:p.Pro121=
NM_004985.5:c.363T>G MANE Select	NP_004976.2:p.Pro121=
NM_033360.4:c.363T>G MANE Plus Clinical	NP_203524.1:p.Pro121=