Canonical Allele Identifier: CA478889993

Gene: KRAS

Linked Data

• dbSNP Id: rs2141505570
• gnomAD v4: 12-25225623-C-T
• COSMIC: COSM5369685
• MyVariant Identifiers: chr12:g.25378557C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25225623C>T , CM000674.2:g.25225623C>T	GRCh38
NC_000012.11:g.25378557C>T , CM000674.1:g.25378557C>T	GRCh37
NC_000012.10:g.25269824C>T	NCBI36
NG_007524.1:g.30298G>A
NG_007524.2:g.30381G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000557334.6:c.112-15712G>A	ENSP00000452512.1:n.112-15712G>A
ENST00000685328.1:c.441G>A	ENSP00000508921.1:p.Lys147=
ENST00000686877.1:c.*412G>A	ENSP00000510431.1:n.*412G>A
ENST00000687356.1:c.*139G>A	ENSP00000510511.1:n.*139G>A
ENST00000688228.1:n.915G>A
ENST00000688940.1:c.441G>A	ENSP00000509238.1:p.Lys147=
ENST00000690406.1:c.151G>A
ENST00000690804.1:c.*402G>A	ENSP00000508568.1:n.*402G>A
ENST00000692768.1:c.243G>A	ENSP00000510254.1:p.Lys81=
ENST00000693229.1:c.366G>A	ENSP00000509223.1:p.Lys122=
ENST00000256078.10:c.441G>A MANE Plus Clinical	ENSP00000256078.5:p.Lys147=
ENST00000311936.8:c.441G>A MANE Select	ENSP00000308495.3:p.Lys147=
ENST00000256078.8:c.441G>A	ENSP00000256078.4:p.Lys147=
ENST00000311936.7:c.441G>A	ENSP00000308495.3:p.Lys147=
ENST00000557334.5:c.112-15712G>A	ENSP00000452512.1:n.112-15712G>A
NM_004985.4:c.441G>A	NP_004976.2:p.Lys147=
NM_033360.3:c.441G>A	NP_203524.1:p.Lys147=
XM_006719069.2:c.441G>A	XP_006719132.1:p.Lys147=
XM_011520653.1:c.441G>A	XP_011518955.1:p.Lys147=
XM_006719069.4:c.441G>A	XP_006719132.1:p.Lys147=
XM_011520653.3:c.441G>A	XP_011518955.1:p.Lys147=
NM_001369786.1:c.441G>A	NP_001356715.1:p.Lys147=
NM_001369787.1:c.441G>A	NP_001356716.1:p.Lys147=
NM_004985.5:c.441G>A MANE Select	NP_004976.2:p.Lys147=
NM_033360.4:c.441G>A MANE Plus Clinical	NP_203524.1:p.Lys147=