Canonical Allele Identifier: CA10641642

Linked Data

ClinVar Variation Id: 308069
dbSNP Id: rs142323886

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25206120_25206121dup , CM000674.2:g.25206120_25206121dup GRCh38
NC_000012.11:g.25359054_25359055dup , CM000674.1:g.25359054_25359055dup GRCh37
NC_000012.10:g.25250321_25250322dup NCBI36
NG_007524.1:g.49808_49809dup
NG_007524.2:g.49891_49892dup

Transcript Alleles

HGVS Amino-acid change
ENST00000685328.1:c.*3682_*3683dup (KRAS) ENSP00000508921.1:n.*3682_*3683dup
ENST00000686877.1:c.*4220_*4221dup (KRAS) ENSP00000510431.1:n.*4220_*4221dup
ENST00000687356.1:c.*3947_*3948dup (KRAS) ENSP00000510511.1:n.*3947_*3948dup
ENST00000690406.1:c.4052_4053dup (KRAS)
ENST00000692768.1:c.*3682_*3683dup (KRAS) ENSP00000510254.1:n.*3682_*3683dup
ENST00000693229.1:c.*3682_*3683dup (KRAS) ENSP00000509223.1:n.*3682_*3683dup
ENST00000256078.10:c.*3803_*3804dup (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*3803_*3804dup
ENST00000311936.8:c.*3682_*3683dup (KRAS) MANE Select ENSP00000308495.3:n.*3682_*3683dup
ENST00000553788.6:c.51+2113_51+2114dup (ETFRF1) ENSP00000451938.2:n.51+2113_51+2114dup
ENST00000311936.7:c.*3682_*3683dup (KRAS) ENSP00000308495.3:n.*3682_*3683dup
ENST00000553788.5:c.45+2113_45+2114dup (ETFRF1) ENSP00000451938.1:n.45+2113_45+2114dup
NM_004985.4:c.*3682_*3683dup (KRAS) NP_004976.2:n.*3682_*3683dup
NM_033360.3:c.*3803_*3804dup (KRAS) NP_203524.1:n.*3803_*3804dup
XM_011520653.1:c.*3682_*3683dup (KRAS) XP_011518955.1:n.*3682_*3683dup
XM_011520653.3:c.*3682_*3683dup (KRAS) XP_011518955.1:n.*3682_*3683dup
NM_001369786.1:c.*3803_*3804dup (KRAS) NP_001356715.1:n.*3803_*3804dup
NM_001369787.1:c.*3682_*3683dup (KRAS) NP_001356716.1:n.*3682_*3683dup
NM_004985.5:c.*3682_*3683dup (KRAS) MANE Select NP_004976.2:n.*3682_*3683dup
NM_033360.4:c.*3803_*3804dup (KRAS) MANE Plus Clinical NP_203524.1:n.*3803_*3804dup