Canonical Allele Identifier: CA384157328

Gene: KRAS

Linked Data

• ClinVar Variation Id: 1711031
• ClinVar RCV Id: RCV002292318
• MyVariant Identifiers: chr12:g.25398242T>G (hg19) ; chr12:g.25245308T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25245308T>G , CM000674.2:g.25245308T>G	GRCh38
NC_000012.11:g.25398242T>G , CM000674.1:g.25398242T>G	GRCh37
NC_000012.10:g.25289509T>G	NCBI36
NG_007524.1:g.10613A>C
NG_007524.2:g.10696A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556131.2:c.77A>C	ENSP00000451856.1:p.Asn26Thr
ENST00000557334.6:c.77A>C	ENSP00000452512.1:p.Asn26Thr
ENST00000685328.1:c.77A>C	ENSP00000508921.1:p.Asn26Thr
ENST00000686877.1:c.77A>C	ENSP00000510431.1:p.Asn26Thr
ENST00000686969.1:c.77A>C	ENSP00000510479.1:p.Asn26Thr
ENST00000687356.1:c.77A>C	ENSP00000510511.1:p.Asn26Thr
ENST00000688940.1:c.77A>C	ENSP00000509238.1:p.Asn26Thr
ENST00000690804.1:c.77A>C	ENSP00000508568.1:p.Asn26Thr
ENST00000692768.1:c.-88+5443A>C	ENSP00000510254.1:n.-88+5443A>C
ENST00000693229.1:c.77A>C	ENSP00000509223.1:p.Asn26Thr
ENST00000256078.10:c.77A>C MANE Plus Clinical	ENSP00000256078.5:p.Asn26Thr
ENST00000311936.8:c.77A>C MANE Select	ENSP00000308495.3:p.Asn26Thr
ENST00000256078.8:c.77A>C	ENSP00000256078.4:p.Asn26Thr
ENST00000311936.7:c.77A>C	ENSP00000308495.3:p.Asn26Thr
ENST00000556131.1:c.77A>C	ENSP00000451856.1:p.Asn26Thr
ENST00000557334.5:c.77A>C	ENSP00000452512.1:p.Asn26Thr
NM_004985.4:c.77A>C	NP_004976.2:p.Asn26Thr
NM_033360.3:c.77A>C	NP_203524.1:p.Asn26Thr
XM_006719069.2:c.77A>C	XP_006719132.1:p.Asn26Thr
XM_011520653.1:c.77A>C	XP_011518955.1:p.Asn26Thr
XM_006719069.4:c.77A>C	XP_006719132.1:p.Asn26Thr
XM_011520653.3:c.77A>C	XP_011518955.1:p.Asn26Thr
NM_001369786.1:c.77A>C	NP_001356715.1:p.Asn26Thr
NM_001369787.1:c.77A>C	NP_001356716.1:p.Asn26Thr
NM_004985.5:c.77A>C MANE Select	NP_004976.2:p.Asn26Thr
NM_033360.4:c.77A>C MANE Plus Clinical	NP_203524.1:p.Asn26Thr