Canonical Allele Identifier: CA384148386

Gene: KRAS

Linked Data

• gnomAD v4: 12-25209842-C-G
• MyVariant Identifiers: chr12:g.25362776C>G (hg19) ; chr12:g.25209842C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209842C>G , CM000674.2:g.25209842C>G	GRCh38
NC_000012.11:g.25362776C>G , CM000674.1:g.25362776C>G	GRCh37
NC_000012.10:g.25254043C>G	NCBI36
NG_007524.1:g.46079G>C
NG_007524.2:g.46162G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.181G>C	ENSP00000452512.1:p.Gly61Arg
ENST00000685328.1:c.520G>C	ENSP00000508921.1:p.Gly174Arg
ENST00000686877.1:c.*491G>C	ENSP00000510431.1:n.*491G>C
ENST00000687356.1:c.*218G>C	ENSP00000510511.1:n.*218G>C
ENST00000688228.1:n.994G>C
ENST00000688940.1:c.520G>C	ENSP00000509238.1:p.Gly174Arg
ENST00000690406.1:c.323G>C
ENST00000690804.1:c.*481G>C	ENSP00000508568.1:n.*481G>C
ENST00000692768.1:c.322G>C	ENSP00000510254.1:p.Gly108Arg
ENST00000693229.1:c.445G>C	ENSP00000509223.1:p.Gly149Arg
ENST00000256078.10:c.*74G>C MANE Plus Clinical	ENSP00000256078.5:n.*74G>C
ENST00000311936.8:c.520G>C MANE Select	ENSP00000308495.3:p.Gly174Arg
ENST00000256078.8:c.*74G>C	ENSP00000256078.4:n.*74G>C
ENST00000311936.7:c.520G>C	ENSP00000308495.3:p.Gly174Arg
ENST00000557334.5:c.181G>C	ENSP00000452512.1:p.Gly61Arg
NM_004985.4:c.520G>C	NP_004976.2:p.Gly174Arg
NM_033360.3:c.*74G>C	NP_203524.1:n.*74G>C
XM_006719069.2:c.*74G>C	XP_006719132.1:n.*74G>C
XM_011520653.1:c.520G>C	XP_011518955.1:p.Gly174Arg
XM_006719069.4:c.*74G>C	XP_006719132.1:n.*74G>C
XM_011520653.3:c.520G>C	XP_011518955.1:p.Gly174Arg
NM_001369786.1:c.*74G>C	NP_001356715.1:n.*74G>C
NM_001369787.1:c.520G>C	NP_001356716.1:p.Gly174Arg
NM_004985.5:c.520G>C MANE Select	NP_004976.2:p.Gly174Arg
NM_033360.4:c.*74G>C MANE Plus Clinical	NP_203524.1:n.*74G>C