Canonical Allele Identifier: CA6486814

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308118
• ClinVar RCV Id: RCV001813461
• dbSNP Id: rs9266
• ExAC: 12:25362217 A / G
• gnomAD v2: 12-25362217-A-G
• gnomAD v3: 12-25209283-A-G
• gnomAD v4: 12-25209283-A-G
• MyVariant Identifiers: chr12:g.25362217A>G (hg19) ; chr12:g.25209283A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209283A>G , CM000674.2:g.25209283A>G	GRCh38
NC_000012.11:g.25362217A>G , CM000674.1:g.25362217A>G	GRCh37
NC_000012.10:g.25253484A>G	NCBI36
NG_007524.1:g.46638T>C
NG_007524.2:g.46721T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*512T>C (KRAS)	ENSP00000452512.1:n.*512T>C
ENST00000685328.1:c.*512T>C (KRAS)	ENSP00000508921.1:n.*512T>C
ENST00000686877.1:c.*1050T>C (KRAS)	ENSP00000510431.1:n.*1050T>C
ENST00000687356.1:c.*777T>C (KRAS)	ENSP00000510511.1:n.*777T>C
ENST00000688940.1:c.*512T>C (KRAS)	ENSP00000509238.1:n.*512T>C
ENST00000690406.1:c.882T>C (KRAS)
ENST00000690804.1:c.*1040T>C (KRAS)	ENSP00000508568.1:n.*1040T>C
ENST00000692768.1:c.*512T>C (KRAS)	ENSP00000510254.1:n.*512T>C
ENST00000693229.1:c.*512T>C (KRAS)	ENSP00000509223.1:n.*512T>C
ENST00000256078.10:c.*633T>C (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*633T>C
ENST00000311936.8:c.*512T>C (KRAS) MANE Select	ENSP00000308495.3:n.*512T>C
ENST00000553788.6:c.*20A>G (ETFRF1)	ENSP00000451938.2:n.*20A>G
ENST00000311936.7:c.*512T>C (KRAS)	ENSP00000308495.3:n.*512T>C
ENST00000553788.5:c.*20A>G (ETFRF1)	ENSP00000451938.1:n.*20A>G
ENST00000557334.5:c.*512T>C (KRAS)	ENSP00000452512.1:n.*512T>C
NM_004985.4:c.*512T>C (KRAS)	NP_004976.2:n.*512T>C
NM_033360.3:c.*633T>C (KRAS)	NP_203524.1:n.*633T>C
XM_011520653.1:c.*512T>C (KRAS)	XP_011518955.1:n.*512T>C
XM_011520653.3:c.*512T>C (KRAS)	XP_011518955.1:n.*512T>C
NM_001369786.1:c.*633T>C (KRAS)	NP_001356715.1:n.*633T>C
NM_001369787.1:c.*512T>C (KRAS)	NP_001356716.1:n.*512T>C
NM_004985.5:c.*512T>C (KRAS) MANE Select	NP_004976.2:n.*512T>C
NM_033360.4:c.*633T>C (KRAS) MANE Plus Clinical	NP_203524.1:n.*633T>C