Canonical Allele Identifier: CA2022884486

Gene: KRAS

Linked Data

• dbSNP Id: rs1951183111

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209775G>T , CM000674.2:g.25209775G>T	GRCh38
NC_000012.11:g.25362709G>T , CM000674.1:g.25362709G>T	GRCh37
NC_000012.10:g.25253976G>T	NCBI36
NG_007524.1:g.46146C>A
NG_007524.2:g.46229C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.*20C>A	ENSP00000452512.1:n.*20C>A
ENST00000685328.1:c.*20C>A	ENSP00000508921.1:n.*20C>A
ENST00000686877.1:c.*558C>A	ENSP00000510431.1:n.*558C>A
ENST00000687356.1:c.*285C>A	ENSP00000510511.1:n.*285C>A
ENST00000688228.1:n.1061C>A
ENST00000688940.1:c.*20C>A	ENSP00000509238.1:n.*20C>A
ENST00000690406.1:c.390C>A
ENST00000690804.1:c.*548C>A	ENSP00000508568.1:n.*548C>A
ENST00000692768.1:c.*20C>A	ENSP00000510254.1:n.*20C>A
ENST00000693229.1:c.*20C>A	ENSP00000509223.1:n.*20C>A
ENST00000256078.10:c.*141C>A MANE Plus Clinical	ENSP00000256078.5:n.*141C>A
ENST00000311936.8:c.*20C>A MANE Select	ENSP00000308495.3:n.*20C>A
ENST00000256078.8:c.*141C>A	ENSP00000256078.4:n.*141C>A
ENST00000311936.7:c.*20C>A	ENSP00000308495.3:n.*20C>A
ENST00000557334.5:c.*20C>A	ENSP00000452512.1:n.*20C>A
NM_004985.4:c.*20C>A	NP_004976.2:n.*20C>A
NM_033360.3:c.*141C>A	NP_203524.1:n.*141C>A
XM_011520653.1:c.*20C>A	XP_011518955.1:n.*20C>A
XM_011520653.3:c.*20C>A	XP_011518955.1:n.*20C>A
NM_001369786.1:c.*141C>A	NP_001356715.1:n.*141C>A
NM_001369787.1:c.*20C>A	NP_001356716.1:n.*20C>A
NM_004985.5:c.*20C>A MANE Select	NP_004976.2:n.*20C>A
NM_033360.4:c.*141C>A MANE Plus Clinical	NP_203524.1:n.*141C>A