Canonical Allele Identifier: CA384148494

Gene: KRAS

Linked Data

• dbSNP Id: rs1951184637
• gnomAD v4: 12-25209889-G-A
• MyVariant Identifiers: chr12:g.25362823G>A (hg19) ; chr12:g.25209889G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209889G>A , CM000674.2:g.25209889G>A	GRCh38
NC_000012.11:g.25362823G>A , CM000674.1:g.25362823G>A	GRCh37
NC_000012.10:g.25254090G>A	NCBI36
NG_007524.1:g.46032C>T
NG_007524.2:g.46115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.134C>T	ENSP00000452512.1:p.Thr45Ile
ENST00000685328.1:c.473C>T	ENSP00000508921.1:p.Thr158Ile
ENST00000686877.1:c.*444C>T	ENSP00000510431.1:n.*444C>T
ENST00000687356.1:c.*171C>T	ENSP00000510511.1:n.*171C>T
ENST00000688228.1:n.947C>T
ENST00000688940.1:c.473C>T	ENSP00000509238.1:p.Thr158Ile
ENST00000690406.1:c.276C>T
ENST00000690804.1:c.*434C>T	ENSP00000508568.1:n.*434C>T
ENST00000692768.1:c.275C>T	ENSP00000510254.1:p.Thr92Ile
ENST00000693229.1:c.398C>T	ENSP00000509223.1:p.Thr133Ile
ENST00000256078.10:c.*27C>T MANE Plus Clinical	ENSP00000256078.5:n.*27C>T
ENST00000311936.8:c.473C>T MANE Select	ENSP00000308495.3:p.Thr158Ile
ENST00000256078.8:c.*27C>T	ENSP00000256078.4:n.*27C>T
ENST00000311936.7:c.473C>T	ENSP00000308495.3:p.Thr158Ile
ENST00000557334.5:c.134C>T	ENSP00000452512.1:p.Thr45Ile
NM_004985.4:c.473C>T	NP_004976.2:p.Thr158Ile
NM_033360.3:c.*27C>T	NP_203524.1:n.*27C>T
XM_006719069.2:c.*27C>T	XP_006719132.1:n.*27C>T
XM_011520653.1:c.473C>T	XP_011518955.1:p.Thr158Ile
XM_006719069.4:c.*27C>T	XP_006719132.1:n.*27C>T
XM_011520653.3:c.473C>T	XP_011518955.1:p.Thr158Ile
NM_001369786.1:c.*27C>T	NP_001356715.1:n.*27C>T
NM_001369787.1:c.473C>T	NP_001356716.1:p.Thr158Ile
NM_004985.5:c.473C>T MANE Select	NP_004976.2:p.Thr158Ile
NM_033360.4:c.*27C>T MANE Plus Clinical	NP_203524.1:n.*27C>T