Canonical Allele Identifier: CA384148340
Gene: KRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25209824T>G , CM000674.2:g.25209824T>G GRCh38
NC_000012.11:g.25362758T>G , CM000674.1:g.25362758T>G GRCh37
NC_000012.10:g.25254025T>G NCBI36
NG_007524.1:g.46097A>C
NG_007524.2:g.46180A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000557334.6:c.199A>C ENSP00000452512.1:p.Lys67Gln
ENST00000685328.1:c.538A>C ENSP00000508921.1:p.Lys180Gln
ENST00000686877.1:c.*509A>C ENSP00000510431.1:n.*509A>C
ENST00000687356.1:c.*236A>C ENSP00000510511.1:n.*236A>C
ENST00000688228.1:n.1012A>C
ENST00000688940.1:c.538A>C ENSP00000509238.1:p.Lys180Gln
ENST00000690406.1:c.341A>C
ENST00000690804.1:c.*499A>C ENSP00000508568.1:n.*499A>C
ENST00000692768.1:c.340A>C ENSP00000510254.1:p.Lys114Gln
ENST00000693229.1:c.463A>C ENSP00000509223.1:p.Lys155Gln
ENST00000256078.10:c.*92A>C MANE Plus Clinical ENSP00000256078.5:n.*92A>C
ENST00000311936.8:c.538A>C MANE Select ENSP00000308495.3:p.Lys180Gln
ENST00000256078.8:c.*92A>C ENSP00000256078.4:n.*92A>C
ENST00000311936.7:c.538A>C ENSP00000308495.3:p.Lys180Gln
ENST00000557334.5:c.199A>C ENSP00000452512.1:p.Lys67Gln
NM_004985.4:c.538A>C NP_004976.2:p.Lys180Gln
NM_033360.3:c.*92A>C NP_203524.1:n.*92A>C
XM_011520653.1:c.538A>C XP_011518955.1:p.Lys180Gln
XM_011520653.3:c.538A>C XP_011518955.1:p.Lys180Gln
NM_001369786.1:c.*92A>C NP_001356715.1:n.*92A>C
NM_001369787.1:c.538A>C NP_001356716.1:p.Lys180Gln
NM_004985.5:c.538A>C MANE Select NP_004976.2:p.Lys180Gln
NM_033360.4:c.*92A>C MANE Plus Clinical NP_203524.1:n.*92A>C