Canonical Allele Identifier: CA384151056
Gene: KRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2752227
ClinVar RCV Id: RCV003540291
MyVariant Identifiers: chr12:g.25378557C>A (hg19) chr12:g.25225623C>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.112-15712G>T ENSP00000452512.1:n.112-15712G>T
ENST00000685328.1:c.441G>T ENSP00000508921.1:p.Lys147Asn
ENST00000686877.1:c.*412G>T ENSP00000510431.1:n.*412G>T
ENST00000687356.1:c.*139G>T ENSP00000510511.1:n.*139G>T
ENST00000688228.1:n.915G>T
ENST00000688940.1:c.441G>T ENSP00000509238.1:p.Lys147Asn
ENST00000690406.1:c.151G>T
ENST00000690804.1:c.*402G>T ENSP00000508568.1:n.*402G>T
ENST00000692768.1:c.243G>T ENSP00000510254.1:p.Lys81Asn
ENST00000693229.1:c.366G>T ENSP00000509223.1:p.Lys122Asn
ENST00000256078.10:c.441G>T MANE Plus Clinical ENSP00000256078.5:p.Lys147Asn
ENST00000311936.8:c.441G>T MANE Select ENSP00000308495.3:p.Lys147Asn
ENST00000256078.8:c.441G>T ENSP00000256078.4:p.Lys147Asn
ENST00000311936.7:c.441G>T ENSP00000308495.3:p.Lys147Asn
ENST00000557334.5:c.112-15712G>T ENSP00000452512.1:n.112-15712G>T
NM_004985.4:c.441G>T NP_004976.2:p.Lys147Asn
NM_033360.3:c.441G>T NP_203524.1:p.Lys147Asn
XM_006719069.2:c.441G>T XP_006719132.1:p.Lys147Asn
XM_011520653.1:c.441G>T XP_011518955.1:p.Lys147Asn
XM_006719069.4:c.441G>T XP_006719132.1:p.Lys147Asn
XM_011520653.3:c.441G>T XP_011518955.1:p.Lys147Asn
NM_001369786.1:c.441G>T NP_001356715.1:p.Lys147Asn
NM_001369787.1:c.441G>T NP_001356716.1:p.Lys147Asn
NM_004985.5:c.441G>T MANE Select NP_004976.2:p.Lys147Asn
NM_033360.4:c.441G>T MANE Plus Clinical NP_203524.1:p.Lys147Asn
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