Canonical Allele Identifier: CA10641649

Gene: KRAS ETFRF1

Linked Data

• ClinVar Variation Id: 308077
• ClinVar RCV Id: RCV000304310
• dbSNP Id: rs34176876
• gnomAD v2: 12-25359464-TA-T
• gnomAD v3: 12-25206530-TA-T
• gnomAD v4: 12-25206530-TA-T
• COSMIC: COSN20109363 ; COSN20109364 ; COSN20109365 ; COSN20109366
• MyVariant Identifiers: chr12:g.25359465del (hg19) ; chr12:g.25206531del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206532del , CM000674.2:g.25206532del	GRCh38
NC_000012.11:g.25359466del , CM000674.1:g.25359466del	GRCh37
NC_000012.10:g.25250733del	NCBI36
NG_007524.1:g.49390del
NG_007524.2:g.49473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3264del (KRAS)	ENSP00000508921.1:n.*3264del
ENST00000686877.1:c.*3802del (KRAS)	ENSP00000510431.1:n.*3802del
ENST00000687356.1:c.*3529del (KRAS)	ENSP00000510511.1:n.*3529del
ENST00000690406.1:c.3634del (KRAS)
ENST00000692768.1:c.*3264del (KRAS)	ENSP00000510254.1:n.*3264del
ENST00000693229.1:c.*3264del (KRAS)	ENSP00000509223.1:n.*3264del
ENST00000256078.10:c.*3385del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3385del
ENST00000311936.8:c.*3264del (KRAS) MANE Select	ENSP00000308495.3:n.*3264del
ENST00000553788.6:c.51+2525del (ETFRF1)	ENSP00000451938.2:n.51+2525del
ENST00000311936.7:c.*3264del (KRAS)	ENSP00000308495.3:n.*3264del
ENST00000553788.5:c.45+2525del (ETFRF1)	ENSP00000451938.1:n.45+2525del
NM_004985.4:c.*3264del (KRAS)	NP_004976.2:n.*3264del
NM_033360.3:c.*3385del (KRAS)	NP_203524.1:n.*3385del
XM_011520653.1:c.*3264del (KRAS)	XP_011518955.1:n.*3264del
XM_011520653.3:c.*3264del (KRAS)	XP_011518955.1:n.*3264del
NM_001369786.1:c.*3385del (KRAS)	NP_001356715.1:n.*3385del
NM_001369787.1:c.*3264del (KRAS)	NP_001356716.1:n.*3264del
NM_004985.5:c.*3264del (KRAS) MANE Select	NP_004976.2:n.*3264del
NM_033360.4:c.*3385del (KRAS) MANE Plus Clinical	NP_203524.1:n.*3385del