Canonical Allele Identifier: CA384148296

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209805-A-G
• MyVariant Identifiers: chr12:g.25362739A>G (hg19) ; chr12:g.25209805A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209805A>G , CM000674.2:g.25209805A>G	GRCh38
NC_000012.11:g.25362739A>G , CM000674.1:g.25362739A>G	GRCh37
NC_000012.10:g.25254006A>G	NCBI36
NG_007524.1:g.46116T>C
NG_007524.2:g.46199T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.218T>C	ENSP00000452512.1:p.Val73Ala
ENST00000685328.1:c.557T>C	ENSP00000508921.1:p.Val186Ala
ENST00000686877.1:c.*528T>C	ENSP00000510431.1:n.*528T>C
ENST00000687356.1:c.*255T>C	ENSP00000510511.1:n.*255T>C
ENST00000688228.1:n.1031T>C
ENST00000688940.1:c.557T>C	ENSP00000509238.1:p.Val186Ala
ENST00000690406.1:c.360T>C
ENST00000690804.1:c.*518T>C	ENSP00000508568.1:n.*518T>C
ENST00000692768.1:c.359T>C	ENSP00000510254.1:p.Val120Ala
ENST00000693229.1:c.482T>C	ENSP00000509223.1:p.Val161Ala
ENST00000256078.10:c.*111T>C MANE Plus Clinical	ENSP00000256078.5:n.*111T>C
ENST00000311936.8:c.557T>C MANE Select	ENSP00000308495.3:p.Val186Ala
ENST00000256078.8:c.*111T>C	ENSP00000256078.4:n.*111T>C
ENST00000311936.7:c.557T>C	ENSP00000308495.3:p.Val186Ala
ENST00000557334.5:c.218T>C	ENSP00000452512.1:p.Val73Ala
NM_004985.4:c.557T>C	NP_004976.2:p.Val186Ala
NM_033360.3:c.*111T>C	NP_203524.1:n.*111T>C
XM_011520653.1:c.557T>C	XP_011518955.1:p.Val186Ala
XM_011520653.3:c.557T>C	XP_011518955.1:p.Val186Ala
NM_001369786.1:c.*111T>C	NP_001356715.1:n.*111T>C
NM_001369787.1:c.557T>C	NP_001356716.1:p.Val186Ala
NM_004985.5:c.557T>C MANE Select	NP_004976.2:p.Val186Ala
NM_033360.4:c.*111T>C MANE Plus Clinical	NP_203524.1:n.*111T>C