Canonical Allele Identifier: CA234205849

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 2642796
• ClinVar RCV Id: RCV003390198
• dbSNP Id: rs988374263
• gnomAD v2: 12-25361095-T-C
• gnomAD v3: 12-25208161-T-C
• gnomAD v4: 12-25208161-T-C
• MyVariant Identifiers: chr12:g.25361095T>C (hg19) ; chr12:g.25208161T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25208161T>C , CM000674.2:g.25208161T>C	GRCh38
NC_000012.11:g.25361095T>C , CM000674.1:g.25361095T>C	GRCh37
NC_000012.10:g.25252362T>C	NCBI36
NG_007524.1:g.47760A>G
NG_007524.2:g.47843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*1634A>G (KRAS)	ENSP00000508921.1:n.*1634A>G
ENST00000686877.1:c.*2172A>G (KRAS)	ENSP00000510431.1:n.*2172A>G
ENST00000687356.1:c.*1899A>G (KRAS)	ENSP00000510511.1:n.*1899A>G
ENST00000688940.1:c.*1634A>G (KRAS)	ENSP00000509238.1:n.*1634A>G
ENST00000690406.1:c.2004A>G (KRAS)
ENST00000690804.1:c.*2162A>G (KRAS)	ENSP00000508568.1:n.*2162A>G
ENST00000692768.1:c.*1634A>G (KRAS)	ENSP00000510254.1:n.*1634A>G
ENST00000693229.1:c.*1634A>G (KRAS)	ENSP00000509223.1:n.*1634A>G
ENST00000256078.10:c.*1755A>G (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*1755A>G
ENST00000311936.8:c.*1634A>G (KRAS) MANE Select	ENSP00000308495.3:n.*1634A>G
ENST00000553788.6:c.52-1034T>C (ETFRF1)	ENSP00000451938.2:n.52-1034T>C
ENST00000311936.7:c.*1634A>G (KRAS)	ENSP00000308495.3:n.*1634A>G
ENST00000553788.5:c.46-1034T>C (ETFRF1)	ENSP00000451938.1:n.46-1034T>C
NM_004985.4:c.*1634A>G (KRAS)	NP_004976.2:n.*1634A>G
NM_033360.3:c.*1755A>G (KRAS)	NP_203524.1:n.*1755A>G
XM_011520653.1:c.*1634A>G (KRAS)	XP_011518955.1:n.*1634A>G
XM_011520653.3:c.*1634A>G (KRAS)	XP_011518955.1:n.*1634A>G
NM_001369786.1:c.*1755A>G (KRAS)	NP_001356715.1:n.*1755A>G
NM_001369787.1:c.*1634A>G (KRAS)	NP_001356716.1:n.*1634A>G
NM_004985.5:c.*1634A>G (KRAS) MANE Select	NP_004976.2:n.*1634A>G
NM_033360.4:c.*1755A>G (KRAS) MANE Plus Clinical	NP_203524.1:n.*1755A>G