Canonical Allele Identifier: CA384148316

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362748G>A (hg19) ; chr12:g.25209814G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209814G>A , CM000674.2:g.25209814G>A	GRCh38
NC_000012.11:g.25362748G>A , CM000674.1:g.25362748G>A	GRCh37
NC_000012.10:g.25254015G>A	NCBI36
NG_007524.1:g.46107C>T
NG_007524.2:g.46190C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.209C>T	ENSP00000452512.1:p.Thr70Ile
ENST00000685328.1:c.548C>T	ENSP00000508921.1:p.Thr183Ile
ENST00000686877.1:c.*519C>T	ENSP00000510431.1:n.*519C>T
ENST00000687356.1:c.*246C>T	ENSP00000510511.1:n.*246C>T
ENST00000688228.1:n.1022C>T
ENST00000688940.1:c.548C>T	ENSP00000509238.1:p.Thr183Ile
ENST00000690406.1:c.351C>T
ENST00000690804.1:c.*509C>T	ENSP00000508568.1:n.*509C>T
ENST00000692768.1:c.350C>T	ENSP00000510254.1:p.Thr117Ile
ENST00000693229.1:c.473C>T	ENSP00000509223.1:p.Thr158Ile
ENST00000256078.10:c.*102C>T MANE Plus Clinical	ENSP00000256078.5:n.*102C>T
ENST00000311936.8:c.548C>T MANE Select	ENSP00000308495.3:p.Thr183Ile
ENST00000256078.8:c.*102C>T	ENSP00000256078.4:n.*102C>T
ENST00000311936.7:c.548C>T	ENSP00000308495.3:p.Thr183Ile
ENST00000557334.5:c.209C>T	ENSP00000452512.1:p.Thr70Ile
NM_004985.4:c.548C>T	NP_004976.2:p.Thr183Ile
NM_033360.3:c.*102C>T	NP_203524.1:n.*102C>T
XM_011520653.1:c.548C>T	XP_011518955.1:p.Thr183Ile
XM_011520653.3:c.548C>T	XP_011518955.1:p.Thr183Ile
NM_001369786.1:c.*102C>T	NP_001356715.1:n.*102C>T
NM_001369787.1:c.548C>T	NP_001356716.1:p.Thr183Ile
NM_004985.5:c.548C>T MANE Select	NP_004976.2:p.Thr183Ile
NM_033360.4:c.*102C>T MANE Plus Clinical	NP_203524.1:n.*102C>T