Canonical Allele Identifier: CA478890242

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25380182A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25227248A>G , CM000674.2:g.25227248A>G	GRCh38
NC_000012.11:g.25380182A>G , CM000674.1:g.25380182A>G	GRCh37
NC_000012.10:g.25271449A>G	NCBI36
NG_007524.1:g.28673T>C
NG_007524.2:g.28756T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.112-17337T>C	ENSP00000452512.1:n.112-17337T>C
ENST00000685328.1:c.276T>C	ENSP00000508921.1:p.Asp92=
ENST00000686877.1:c.*247T>C	ENSP00000510431.1:n.*247T>C
ENST00000687356.1:c.112-1475T>C	ENSP00000510511.1:n.112-1475T>C
ENST00000688228.1:n.750T>C
ENST00000688940.1:c.276T>C	ENSP00000509238.1:p.Asp92=
ENST00000690804.1:c.*237T>C	ENSP00000508568.1:n.*237T>C
ENST00000692768.1:c.78T>C	ENSP00000510254.1:p.Asp26=
ENST00000693229.1:c.201T>C	ENSP00000509223.1:p.Asp67=
ENST00000256078.10:c.276T>C MANE Plus Clinical	ENSP00000256078.5:p.Asp92=
ENST00000311936.8:c.276T>C MANE Select	ENSP00000308495.3:p.Asp92=
ENST00000256078.8:c.276T>C	ENSP00000256078.4:p.Asp92=
ENST00000311936.7:c.276T>C	ENSP00000308495.3:p.Asp92=
ENST00000557334.5:c.112-17337T>C	ENSP00000452512.1:n.112-17337T>C
NM_004985.4:c.276T>C	NP_004976.2:p.Asp92=
NM_033360.3:c.276T>C	NP_203524.1:p.Asp92=
XM_006719069.2:c.276T>C	XP_006719132.1:p.Asp92=
XM_011520653.1:c.276T>C	XP_011518955.1:p.Asp92=
XM_006719069.4:c.276T>C	XP_006719132.1:p.Asp92=
XM_011520653.3:c.276T>C	XP_011518955.1:p.Asp92=
NM_001369786.1:c.276T>C	NP_001356715.1:p.Asp92=
NM_001369787.1:c.276T>C	NP_001356716.1:p.Asp92=
NM_004985.5:c.276T>C MANE Select	NP_004976.2:p.Asp92=
NM_033360.4:c.276T>C MANE Plus Clinical	NP_203524.1:p.Asp92=