Canonical Allele Identifier: CA2617999601

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.25208229_25208289dup , CM000674.2:g.25208229_25208289dup GRCh38
NC_000012.11:g.25361163_25361223dup , CM000674.1:g.25361163_25361223dup GRCh37
NC_000012.10:g.25252430_25252490dup NCBI36
NG_007524.1:g.47633_47693dup
NG_007524.2:g.47716_47776dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000685328.1:c.*1507_*1567dup (KRAS) ENSP00000508921.1:n.*1507_*1567dup
ENST00000686877.1:c.*2045_*2105dup (KRAS) ENSP00000510431.1:n.*2045_*2105dup
ENST00000687356.1:c.*1772_*1832dup (KRAS) ENSP00000510511.1:n.*1772_*1832dup
ENST00000688940.1:c.*1507_*1567dup (KRAS) ENSP00000509238.1:n.*1507_*1567dup
ENST00000690406.1:c.1877_1937dup (KRAS)
ENST00000690804.1:c.*2035_*2095dup (KRAS) ENSP00000508568.1:n.*2035_*2095dup
ENST00000692768.1:c.*1507_*1567dup (KRAS) ENSP00000510254.1:n.*1507_*1567dup
ENST00000693229.1:c.*1507_*1567dup (KRAS) ENSP00000509223.1:n.*1507_*1567dup
ENST00000256078.10:c.*1628_*1688dup (KRAS) MANE Plus Clinical ENSP00000256078.5:n.*1628_*1688dup
ENST00000311936.8:c.*1507_*1567dup (KRAS) MANE Select ENSP00000308495.3:n.*1507_*1567dup
ENST00000553788.6:c.52-966_52-906dup (ETFRF1) ENSP00000451938.2:n.52-966_52-906dup
ENST00000311936.7:c.*1507_*1567dup (KRAS) ENSP00000308495.3:n.*1507_*1567dup
ENST00000553788.5:c.46-966_46-906dup (ETFRF1) ENSP00000451938.1:n.46-966_46-906dup
NM_004985.4:c.*1507_*1567dup (KRAS) NP_004976.2:n.*1507_*1567dup
NM_033360.3:c.*1628_*1688dup (KRAS) NP_203524.1:n.*1628_*1688dup
XM_011520653.1:c.*1507_*1567dup (KRAS) XP_011518955.1:n.*1507_*1567dup
XM_011520653.3:c.*1507_*1567dup (KRAS) XP_011518955.1:n.*1507_*1567dup
NM_001369786.1:c.*1628_*1688dup (KRAS) NP_001356715.1:n.*1628_*1688dup
NM_001369787.1:c.*1507_*1567dup (KRAS) NP_001356716.1:n.*1507_*1567dup
NM_004985.5:c.*1507_*1567dup (KRAS) MANE Select NP_004976.2:n.*1507_*1567dup
NM_033360.4:c.*1628_*1688dup (KRAS) MANE Plus Clinical NP_203524.1:n.*1628_*1688dup