Canonical Allele Identifier: CA384151249

Gene: KRAS

Linked Data

• MyVariant Identifiers: chr12:g.25378600A>G (hg19) ; chr12:g.25225666A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225666A>G , CM000674.2:g.25225666A>G	GRCh38
NC_000012.11:g.25378600A>G , CM000674.1:g.25378600A>G	GRCh37
NC_000012.10:g.25269867A>G	NCBI36
NG_007524.1:g.30255T>C
NG_007524.2:g.30338T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15755T>C	ENSP00000452512.1:n.112-15755T>C
ENST00000685328.1:c.398T>C	ENSP00000508921.1:p.Leu133Ser
ENST00000686877.1:c.*369T>C	ENSP00000510431.1:n.*369T>C
ENST00000687356.1:c.*96T>C	ENSP00000510511.1:n.*96T>C
ENST00000688228.1:n.872T>C
ENST00000688940.1:c.398T>C	ENSP00000509238.1:p.Leu133Ser
ENST00000690406.1:c.108T>C
ENST00000690804.1:c.*359T>C	ENSP00000508568.1:n.*359T>C
ENST00000692768.1:c.200T>C	ENSP00000510254.1:p.Leu67Ser
ENST00000693229.1:c.323T>C	ENSP00000509223.1:p.Leu108Ser
ENST00000256078.10:c.398T>C MANE Plus Clinical	ENSP00000256078.5:p.Leu133Ser
ENST00000311936.8:c.398T>C MANE Select	ENSP00000308495.3:p.Leu133Ser
ENST00000256078.8:c.398T>C	ENSP00000256078.4:p.Leu133Ser
ENST00000311936.7:c.398T>C	ENSP00000308495.3:p.Leu133Ser
ENST00000557334.5:c.112-15755T>C	ENSP00000452512.1:n.112-15755T>C
NM_004985.4:c.398T>C	NP_004976.2:p.Leu133Ser
NM_033360.3:c.398T>C	NP_203524.1:p.Leu133Ser
XM_006719069.2:c.398T>C	XP_006719132.1:p.Leu133Ser
XM_011520653.1:c.398T>C	XP_011518955.1:p.Leu133Ser
XM_006719069.4:c.398T>C	XP_006719132.1:p.Leu133Ser
XM_011520653.3:c.398T>C	XP_011518955.1:p.Leu133Ser
NM_001369786.1:c.398T>C	NP_001356715.1:p.Leu133Ser
NM_001369787.1:c.398T>C	NP_001356716.1:p.Leu133Ser
NM_004985.5:c.398T>C MANE Select	NP_004976.2:p.Leu133Ser
NM_033360.4:c.398T>C MANE Plus Clinical	NP_203524.1:p.Leu133Ser