Canonical Allele Identifier: CA2617999574

Gene: KRAS ETFRF1

Linked Data

• gnomAD v4: 12-25208166-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208166_25208167insC , CM000674.2:g.25208166_25208167insC	GRCh38
NC_000012.11:g.25361100_25361101insC , CM000674.1:g.25361100_25361101insC	GRCh37
NC_000012.10:g.25252367_25252368insC	NCBI36
NG_007524.1:g.47754_47755insG
NG_007524.2:g.47837_47838insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1628_*1629insG (KRAS)	ENSP00000508921.1:n.*1628_*1629insG
ENST00000686877.1:c.*2166_*2167insG (KRAS)	ENSP00000510431.1:n.*2166_*2167insG
ENST00000687356.1:c.*1893_*1894insG (KRAS)	ENSP00000510511.1:n.*1893_*1894insG
ENST00000688940.1:c.*1628_*1629insG (KRAS)	ENSP00000509238.1:n.*1628_*1629insG
ENST00000690406.1:c.1998_1999insG (KRAS)
ENST00000690804.1:c.*2156_*2157insG (KRAS)	ENSP00000508568.1:n.*2156_*2157insG
ENST00000692768.1:c.*1628_*1629insG (KRAS)	ENSP00000510254.1:n.*1628_*1629insG
ENST00000693229.1:c.*1628_*1629insG (KRAS)	ENSP00000509223.1:n.*1628_*1629insG
ENST00000256078.10:c.*1749_*1750insG (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1749_*1750insG
ENST00000311936.8:c.*1628_*1629insG (KRAS) MANE Select	ENSP00000308495.3:n.*1628_*1629insG
ENST00000553788.6:c.52-1029_52-1028insC (ETFRF1)	ENSP00000451938.2:n.52-1029_52-1028insC
ENST00000311936.7:c.*1628_*1629insG (KRAS)	ENSP00000308495.3:n.*1628_*1629insG
ENST00000553788.5:c.46-1029_46-1028insC (ETFRF1)	ENSP00000451938.1:n.46-1029_46-1028insC
NM_004985.4:c.*1628_*1629insG (KRAS)	NP_004976.2:n.*1628_*1629insG
NM_033360.3:c.*1749_*1750insG (KRAS)	NP_203524.1:n.*1749_*1750insG
XM_011520653.1:c.*1628_*1629insG (KRAS)	XP_011518955.1:n.*1628_*1629insG
XM_011520653.3:c.*1628_*1629insG (KRAS)	XP_011518955.1:n.*1628_*1629insG
NM_001369786.1:c.*1749_*1750insG (KRAS)	NP_001356715.1:n.*1749_*1750insG
NM_001369787.1:c.*1628_*1629insG (KRAS)	NP_001356716.1:n.*1628_*1629insG
NM_004985.5:c.*1628_*1629insG (KRAS) MANE Select	NP_004976.2:n.*1628_*1629insG
NM_033360.4:c.*1749_*1750insG (KRAS) MANE Plus Clinical	NP_203524.1:n.*1749_*1750insG