Canonical Allele Identifier: CA603691307

Gene: KRAS

Linked Data

• dbSNP Id: rs1169193001
• gnomAD v2: 12-25362686-C-G
• gnomAD v4: 12-25209752-C-G
• MyVariant Identifiers: chr12:g.25362686C>G (hg19) ; chr12:g.25209752C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209752C>G , CM000674.2:g.25209752C>G	GRCh38
NC_000012.11:g.25362686C>G , CM000674.1:g.25362686C>G	GRCh37
NC_000012.10:g.25253953C>G	NCBI36
NG_007524.1:g.46169G>C
NG_007524.2:g.46252G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*43G>C	ENSP00000452512.1:n.*43G>C
ENST00000685328.1:c.*43G>C	ENSP00000508921.1:n.*43G>C
ENST00000686877.1:c.*581G>C	ENSP00000510431.1:n.*581G>C
ENST00000687356.1:c.*308G>C	ENSP00000510511.1:n.*308G>C
ENST00000688228.1:n.1084G>C
ENST00000688940.1:c.*43G>C	ENSP00000509238.1:n.*43G>C
ENST00000690406.1:c.413G>C
ENST00000690804.1:c.*571G>C	ENSP00000508568.1:n.*571G>C
ENST00000692768.1:c.*43G>C	ENSP00000510254.1:n.*43G>C
ENST00000693229.1:c.*43G>C	ENSP00000509223.1:n.*43G>C
ENST00000256078.10:c.*164G>C MANE Plus Clinical	ENSP00000256078.5:n.*164G>C
ENST00000311936.8:c.*43G>C MANE Select	ENSP00000308495.3:n.*43G>C
ENST00000256078.8:c.*164G>C	ENSP00000256078.4:n.*164G>C
ENST00000311936.7:c.*43G>C	ENSP00000308495.3:n.*43G>C
ENST00000557334.5:c.*43G>C	ENSP00000452512.1:n.*43G>C
NM_004985.4:c.*43G>C	NP_004976.2:n.*43G>C
NM_033360.3:c.*164G>C	NP_203524.1:n.*164G>C
XM_011520653.1:c.*43G>C	XP_011518955.1:n.*43G>C
XM_011520653.3:c.*43G>C	XP_011518955.1:n.*43G>C
NM_001369786.1:c.*164G>C	NP_001356715.1:n.*164G>C
NM_001369787.1:c.*43G>C	NP_001356716.1:n.*43G>C
NM_004985.5:c.*43G>C MANE Select	NP_004976.2:n.*43G>C
NM_033360.4:c.*164G>C MANE Plus Clinical	NP_203524.1:n.*164G>C