Canonical Allele Identifier: CA384148323

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362750C>G (hg19) ; chr12:g.25209816C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209816C>G , CM000674.2:g.25209816C>G	GRCh38
NC_000012.11:g.25362750C>G , CM000674.1:g.25362750C>G	GRCh37
NC_000012.10:g.25254017C>G	NCBI36
NG_007524.1:g.46105G>C
NG_007524.2:g.46188G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.207G>C	ENSP00000452512.1:p.Lys69Asn
ENST00000685328.1:c.546G>C	ENSP00000508921.1:p.Lys182Asn
ENST00000686877.1:c.*517G>C	ENSP00000510431.1:n.*517G>C
ENST00000687356.1:c.*244G>C	ENSP00000510511.1:n.*244G>C
ENST00000688228.1:n.1020G>C
ENST00000688940.1:c.546G>C	ENSP00000509238.1:p.Lys182Asn
ENST00000690406.1:c.349G>C
ENST00000690804.1:c.*507G>C	ENSP00000508568.1:n.*507G>C
ENST00000692768.1:c.348G>C	ENSP00000510254.1:p.Lys116Asn
ENST00000693229.1:c.471G>C	ENSP00000509223.1:p.Lys157Asn
ENST00000256078.10:c.*100G>C MANE Plus Clinical	ENSP00000256078.5:n.*100G>C
ENST00000311936.8:c.546G>C MANE Select	ENSP00000308495.3:p.Lys182Asn
ENST00000256078.8:c.*100G>C	ENSP00000256078.4:n.*100G>C
ENST00000311936.7:c.546G>C	ENSP00000308495.3:p.Lys182Asn
ENST00000557334.5:c.207G>C	ENSP00000452512.1:p.Lys69Asn
NM_004985.4:c.546G>C	NP_004976.2:p.Lys182Asn
NM_033360.3:c.*100G>C	NP_203524.1:n.*100G>C
XM_011520653.1:c.546G>C	XP_011518955.1:p.Lys182Asn
XM_011520653.3:c.546G>C	XP_011518955.1:p.Lys182Asn
NM_001369786.1:c.*100G>C	NP_001356715.1:n.*100G>C
NM_001369787.1:c.546G>C	NP_001356716.1:p.Lys182Asn
NM_004985.5:c.546G>C MANE Select	NP_004976.2:p.Lys182Asn
NM_033360.4:c.*100G>C MANE Plus Clinical	NP_203524.1:n.*100G>C