Canonical Allele Identifier: CA234205897

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs946847796
• gnomAD v2: 12-25361112-AACT-A
• gnomAD v3: 12-25208178-AACT-A
• gnomAD v4: 12-25208178-AACT-A
• MyVariant Identifiers: chr12:g.25361113_25361115del (hg19) ; chr12:g.25208179_25208181del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208180_25208182del , CM000674.2:g.25208180_25208182del	GRCh38
NC_000012.11:g.25361114_25361116del , CM000674.1:g.25361114_25361116del	GRCh37
NC_000012.10:g.25252381_25252383del	NCBI36
NG_007524.1:g.47740_47742del
NG_007524.2:g.47823_47825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1614_*1616del (KRAS)	ENSP00000508921.1:n.*1614_*1616del
ENST00000686877.1:c.*2152_*2154del (KRAS)	ENSP00000510431.1:n.*2152_*2154del
ENST00000687356.1:c.*1879_*1881del (KRAS)	ENSP00000510511.1:n.*1879_*1881del
ENST00000688940.1:c.*1614_*1616del (KRAS)	ENSP00000509238.1:n.*1614_*1616del
ENST00000690406.1:c.1984_1986del (KRAS)
ENST00000690804.1:c.*2142_*2144del (KRAS)	ENSP00000508568.1:n.*2142_*2144del
ENST00000692768.1:c.*1614_*1616del (KRAS)	ENSP00000510254.1:n.*1614_*1616del
ENST00000693229.1:c.*1614_*1616del (KRAS)	ENSP00000509223.1:n.*1614_*1616del
ENST00000256078.10:c.*1735_*1737del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1735_*1737del
ENST00000311936.8:c.*1614_*1616del (KRAS) MANE Select	ENSP00000308495.3:n.*1614_*1616del
ENST00000553788.6:c.52-1015_52-1013del (ETFRF1)	ENSP00000451938.2:n.52-1015_52-1013del
ENST00000311936.7:c.*1614_*1616del (KRAS)	ENSP00000308495.3:n.*1614_*1616del
ENST00000553788.5:c.46-1015_46-1013del (ETFRF1)	ENSP00000451938.1:n.46-1015_46-1013del
NM_004985.4:c.*1614_*1616del (KRAS)	NP_004976.2:n.*1614_*1616del
NM_033360.3:c.*1735_*1737del (KRAS)	NP_203524.1:n.*1735_*1737del
XM_011520653.1:c.*1614_*1616del (KRAS)	XP_011518955.1:n.*1614_*1616del
XM_011520653.3:c.*1614_*1616del (KRAS)	XP_011518955.1:n.*1614_*1616del
NM_001369786.1:c.*1735_*1737del (KRAS)	NP_001356715.1:n.*1735_*1737del
NM_001369787.1:c.*1614_*1616del (KRAS)	NP_001356716.1:n.*1614_*1616del
NM_004985.5:c.*1614_*1616del (KRAS) MANE Select	NP_004976.2:n.*1614_*1616del
NM_033360.4:c.*1735_*1737del (KRAS) MANE Plus Clinical	NP_203524.1:n.*1735_*1737del