Canonical Allele Identifier: CA478891821

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1711030
• ClinVar RCV Id: RCV002292317
• dbSNP Id: rs2135805909
• MyVariant Identifiers: chr12:g.25398244C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245310C>T , CM000674.2:g.25245310C>T	GRCh38
NC_000012.11:g.25398244C>T , CM000674.1:g.25398244C>T	GRCh37
NC_000012.10:g.25289511C>T	NCBI36
NG_007524.1:g.10611G>A
NG_007524.2:g.10694G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000556131.2:c.75G>A	ENSP00000451856.1:p.Gln25=
ENST00000557334.6:c.75G>A	ENSP00000452512.1:p.Gln25=
ENST00000685328.1:c.75G>A	ENSP00000508921.1:p.Gln25=
ENST00000686877.1:c.75G>A	ENSP00000510431.1:p.Gln25=
ENST00000686969.1:c.75G>A	ENSP00000510479.1:p.Gln25=
ENST00000687356.1:c.75G>A	ENSP00000510511.1:p.Gln25=
ENST00000688940.1:c.75G>A	ENSP00000509238.1:p.Gln25=
ENST00000690804.1:c.75G>A	ENSP00000508568.1:p.Gln25=
ENST00000692768.1:c.-88+5441G>A	ENSP00000510254.1:n.-88+5441G>A
ENST00000693229.1:c.75G>A	ENSP00000509223.1:p.Gln25=
ENST00000256078.10:c.75G>A MANE Plus Clinical	ENSP00000256078.5:p.Gln25=
ENST00000311936.8:c.75G>A MANE Select	ENSP00000308495.3:p.Gln25=
ENST00000256078.8:c.75G>A	ENSP00000256078.4:p.Gln25=
ENST00000311936.7:c.75G>A	ENSP00000308495.3:p.Gln25=
ENST00000556131.1:c.75G>A	ENSP00000451856.1:p.Gln25=
ENST00000557334.5:c.75G>A	ENSP00000452512.1:p.Gln25=
NM_004985.4:c.75G>A	NP_004976.2:p.Gln25=
NM_033360.3:c.75G>A	NP_203524.1:p.Gln25=
XM_006719069.2:c.75G>A	XP_006719132.1:p.Gln25=
XM_011520653.1:c.75G>A	XP_011518955.1:p.Gln25=
XM_006719069.4:c.75G>A	XP_006719132.1:p.Gln25=
XM_011520653.3:c.75G>A	XP_011518955.1:p.Gln25=
NM_001369786.1:c.75G>A	NP_001356715.1:p.Gln25=
NM_001369787.1:c.75G>A	NP_001356716.1:p.Gln25=
NM_004985.5:c.75G>A MANE Select	NP_004976.2:p.Gln25=
NM_033360.4:c.75G>A MANE Plus Clinical	NP_203524.1:p.Gln25=