Canonical Allele Identifier: CA384148477

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362814C>A (hg19) ; chr12:g.25209880C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209880C>A , CM000674.2:g.25209880C>A	GRCh38
NC_000012.11:g.25362814C>A , CM000674.1:g.25362814C>A	GRCh37
NC_000012.10:g.25254081C>A	NCBI36
NG_007524.1:g.46041G>T
NG_007524.2:g.46124G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.143G>T	ENSP00000452512.1:p.Arg48Leu
ENST00000685328.1:c.482G>T	ENSP00000508921.1:p.Arg161Leu
ENST00000686877.1:c.*453G>T	ENSP00000510431.1:n.*453G>T
ENST00000687356.1:c.*180G>T	ENSP00000510511.1:n.*180G>T
ENST00000688228.1:n.956G>T
ENST00000688940.1:c.482G>T	ENSP00000509238.1:p.Arg161Leu
ENST00000690406.1:c.285G>T
ENST00000690804.1:c.*443G>T	ENSP00000508568.1:n.*443G>T
ENST00000692768.1:c.284G>T	ENSP00000510254.1:p.Arg95Leu
ENST00000693229.1:c.407G>T	ENSP00000509223.1:p.Arg136Leu
ENST00000256078.10:c.*36G>T MANE Plus Clinical	ENSP00000256078.5:n.*36G>T
ENST00000311936.8:c.482G>T MANE Select	ENSP00000308495.3:p.Arg161Leu
ENST00000256078.8:c.*36G>T	ENSP00000256078.4:n.*36G>T
ENST00000311936.7:c.482G>T	ENSP00000308495.3:p.Arg161Leu
ENST00000557334.5:c.143G>T	ENSP00000452512.1:p.Arg48Leu
NM_004985.4:c.482G>T	NP_004976.2:p.Arg161Leu
NM_033360.3:c.*36G>T	NP_203524.1:n.*36G>T
XM_006719069.2:c.*36G>T	XP_006719132.1:n.*36G>T
XM_011520653.1:c.482G>T	XP_011518955.1:p.Arg161Leu
XM_006719069.4:c.*36G>T	XP_006719132.1:n.*36G>T
XM_011520653.3:c.482G>T	XP_011518955.1:p.Arg161Leu
NM_001369786.1:c.*36G>T	NP_001356715.1:n.*36G>T
NM_001369787.1:c.482G>T	NP_001356716.1:p.Arg161Leu
NM_004985.5:c.482G>T MANE Select	NP_004976.2:p.Arg161Leu
NM_033360.4:c.*36G>T MANE Plus Clinical	NP_203524.1:n.*36G>T