Canonical Allele Identifier: CA10602360

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 40467
• ClinVar RCV Id: RCV001813239
• dbSNP Id: rs712
• gnomAD v2: 12-25362552-A-C
• gnomAD v3: 12-25209618-A-C
• gnomAD v4: 12-25209618-A-C
• MyVariant Identifiers: chr12:g.25362552A>C (hg19) ; chr12:g.25209618A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25209618A>C , CM000674.2:g.25209618A>C	GRCh38
NC_000012.11:g.25362552A>C , CM000674.1:g.25362552A>C	GRCh37
NC_000012.10:g.25253819A>C	NCBI36
NG_007524.1:g.46303T>G
NG_007524.2:g.46386T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000557334.6:c.*177T>G (KRAS)	ENSP00000452512.1:n.*177T>G
ENST00000685328.1:c.*177T>G (KRAS)	ENSP00000508921.1:n.*177T>G
ENST00000686877.1:c.*715T>G (KRAS)	ENSP00000510431.1:n.*715T>G
ENST00000687356.1:c.*442T>G (KRAS)	ENSP00000510511.1:n.*442T>G
ENST00000688940.1:c.*177T>G (KRAS)	ENSP00000509238.1:n.*177T>G
ENST00000690406.1:c.547T>G (KRAS)
ENST00000690804.1:c.*705T>G (KRAS)	ENSP00000508568.1:n.*705T>G
ENST00000692768.1:c.*177T>G (KRAS)	ENSP00000510254.1:n.*177T>G
ENST00000693229.1:c.*177T>G (KRAS)	ENSP00000509223.1:n.*177T>G
ENST00000256078.10:c.*298T>G (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*298T>G
ENST00000311936.8:c.*177T>G (KRAS) MANE Select	ENSP00000308495.3:n.*177T>G
ENST00000553788.6:c.*355A>C (ETFRF1)	ENSP00000451938.2:n.*355A>C
ENST00000256078.8:c.*298T>G (KRAS)	ENSP00000256078.4:n.*298T>G
ENST00000311936.7:c.*177T>G (KRAS)	ENSP00000308495.3:n.*177T>G
ENST00000553788.5:c.*355A>C (ETFRF1)	ENSP00000451938.1:n.*355A>C
ENST00000557334.5:c.*177T>G (KRAS)	ENSP00000452512.1:n.*177T>G
NM_004985.4:c.*177T>G (KRAS)	NP_004976.2:n.*177T>G
NM_033360.3:c.*298T>G (KRAS)	NP_203524.1:n.*298T>G
XM_011520653.1:c.*177T>G (KRAS)	XP_011518955.1:n.*177T>G
XM_011520653.3:c.*177T>G (KRAS)	XP_011518955.1:n.*177T>G
NM_001369786.1:c.*298T>G (KRAS)	NP_001356715.1:n.*298T>G
NM_001369787.1:c.*177T>G (KRAS)	NP_001356716.1:n.*177T>G
NM_004985.5:c.*177T>G (KRAS) MANE Select	NP_004976.2:n.*177T>G
NM_033360.4:c.*298T>G (KRAS) MANE Plus Clinical	NP_203524.1:n.*298T>G