Canonical Allele Identifier: CA478890057

Gene: KRAS

Linked Data

• dbSNP Id: rs1951384352
• MyVariant Identifiers: chr12:g.25378641A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225707A>G , CM000674.2:g.25225707A>G	GRCh38
NC_000012.11:g.25378641A>G , CM000674.1:g.25378641A>G	GRCh37
NC_000012.10:g.25269908A>G	NCBI36
NG_007524.1:g.30214T>C
NG_007524.2:g.30297T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15796T>C	ENSP00000452512.1:n.112-15796T>C
ENST00000685328.1:c.357T>C	ENSP00000508921.1:p.Asp119=
ENST00000686877.1:c.*328T>C	ENSP00000510431.1:n.*328T>C
ENST00000687356.1:c.*55T>C	ENSP00000510511.1:n.*55T>C
ENST00000688228.1:n.831T>C
ENST00000688940.1:c.357T>C	ENSP00000509238.1:p.Asp119=
ENST00000690406.1:c.67T>C
ENST00000690804.1:c.*318T>C	ENSP00000508568.1:n.*318T>C
ENST00000692768.1:c.159T>C	ENSP00000510254.1:p.Asp53=
ENST00000693229.1:c.282T>C	ENSP00000509223.1:p.Asp94=
ENST00000256078.10:c.357T>C MANE Plus Clinical	ENSP00000256078.5:p.Asp119=
ENST00000311936.8:c.357T>C MANE Select	ENSP00000308495.3:p.Asp119=
ENST00000256078.8:c.357T>C	ENSP00000256078.4:p.Asp119=
ENST00000311936.7:c.357T>C	ENSP00000308495.3:p.Asp119=
ENST00000557334.5:c.112-15796T>C	ENSP00000452512.1:n.112-15796T>C
NM_004985.4:c.357T>C	NP_004976.2:p.Asp119=
NM_033360.3:c.357T>C	NP_203524.1:p.Asp119=
XM_006719069.2:c.357T>C	XP_006719132.1:p.Asp119=
XM_011520653.1:c.357T>C	XP_011518955.1:p.Asp119=
XM_006719069.4:c.357T>C	XP_006719132.1:p.Asp119=
XM_011520653.3:c.357T>C	XP_011518955.1:p.Asp119=
NM_001369786.1:c.357T>C	NP_001356715.1:p.Asp119=
NM_001369787.1:c.357T>C	NP_001356716.1:p.Asp119=
NM_004985.5:c.357T>C MANE Select	NP_004976.2:p.Asp119=
NM_033360.4:c.357T>C MANE Plus Clinical	NP_203524.1:p.Asp119=