Canonical Allele Identifier: CA384148320

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25362749T>G (hg19) ; chr12:g.25209815T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209815T>G , CM000674.2:g.25209815T>G	GRCh38
NC_000012.11:g.25362749T>G , CM000674.1:g.25362749T>G	GRCh37
NC_000012.10:g.25254016T>G	NCBI36
NG_007524.1:g.46106A>C
NG_007524.2:g.46189A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.208A>C	ENSP00000452512.1:p.Thr70Pro
ENST00000685328.1:c.547A>C	ENSP00000508921.1:p.Thr183Pro
ENST00000686877.1:c.*518A>C	ENSP00000510431.1:n.*518A>C
ENST00000687356.1:c.*245A>C	ENSP00000510511.1:n.*245A>C
ENST00000688228.1:n.1021A>C
ENST00000688940.1:c.547A>C	ENSP00000509238.1:p.Thr183Pro
ENST00000690406.1:c.350A>C
ENST00000690804.1:c.*508A>C	ENSP00000508568.1:n.*508A>C
ENST00000692768.1:c.349A>C	ENSP00000510254.1:p.Thr117Pro
ENST00000693229.1:c.472A>C	ENSP00000509223.1:p.Thr158Pro
ENST00000256078.10:c.*101A>C MANE Plus Clinical	ENSP00000256078.5:n.*101A>C
ENST00000311936.8:c.547A>C MANE Select	ENSP00000308495.3:p.Thr183Pro
ENST00000256078.8:c.*101A>C	ENSP00000256078.4:n.*101A>C
ENST00000311936.7:c.547A>C	ENSP00000308495.3:p.Thr183Pro
ENST00000557334.5:c.208A>C	ENSP00000452512.1:p.Thr70Pro
NM_004985.4:c.547A>C	NP_004976.2:p.Thr183Pro
NM_033360.3:c.*101A>C	NP_203524.1:n.*101A>C
XM_011520653.1:c.547A>C	XP_011518955.1:p.Thr183Pro
XM_011520653.3:c.547A>C	XP_011518955.1:p.Thr183Pro
NM_001369786.1:c.*101A>C	NP_001356715.1:n.*101A>C
NM_001369787.1:c.547A>C	NP_001356716.1:p.Thr183Pro
NM_004985.5:c.547A>C MANE Select	NP_004976.2:p.Thr183Pro
NM_033360.4:c.*101A>C MANE Plus Clinical	NP_203524.1:n.*101A>C