Canonical Allele Identifier: CA10637049

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308054
• ClinVar RCV Id: RCV000285443 ; RCV003391091
• dbSNP Id: rs768891600
• gnomAD v2: 12-25358231-A-G
• gnomAD v3: 12-25205297-A-G
• gnomAD v4: 12-25205297-A-G
• MyVariant Identifiers: chr12:g.25358231A>G (hg19) ; chr12:g.25205297A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25205297A>G , CM000674.2:g.25205297A>G	GRCh38
NC_000012.11:g.25358231A>G , CM000674.1:g.25358231A>G	GRCh37
NC_000012.10:g.25249498A>G	NCBI36
NG_007524.1:g.50624T>C
NG_007524.2:g.50707T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*4498T>C (KRAS)	ENSP00000508921.1:n.*4498T>C
ENST00000686877.1:c.*5036T>C (KRAS)	ENSP00000510431.1:n.*5036T>C
ENST00000687356.1:c.*4763T>C (KRAS)	ENSP00000510511.1:n.*4763T>C
ENST00000690406.1:c.4868T>C (KRAS)
ENST00000693229.1:c.*4498T>C (KRAS)	ENSP00000509223.1:n.*4498T>C
ENST00000256078.10:c.*4619T>C (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*4619T>C
ENST00000311936.8:c.*4498T>C (KRAS) MANE Select	ENSP00000308495.3:n.*4498T>C
ENST00000553788.6:c.51+1290A>G (ETFRF1)	ENSP00000451938.2:n.51+1290A>G
ENST00000311936.7:c.*4498T>C (KRAS)	ENSP00000308495.3:n.*4498T>C
ENST00000553788.5:c.45+1290A>G (ETFRF1)	ENSP00000451938.1:n.45+1290A>G
NM_004985.4:c.*4498T>C (KRAS)	NP_004976.2:n.*4498T>C
NM_033360.3:c.*4619T>C (KRAS)	NP_203524.1:n.*4619T>C
XM_011520653.1:c.*4498T>C (KRAS)	XP_011518955.1:n.*4498T>C
XM_011520653.3:c.*4498T>C (KRAS)	XP_011518955.1:n.*4498T>C
NM_001369786.1:c.*4619T>C (KRAS)	NP_001356715.1:n.*4619T>C
NM_001369787.1:c.*4498T>C (KRAS)	NP_001356716.1:n.*4498T>C
NM_004985.5:c.*4498T>C (KRAS) MANE Select	NP_004976.2:n.*4498T>C
NM_033360.4:c.*4619T>C (KRAS) MANE Plus Clinical	NP_203524.1:n.*4619T>C