Canonical Allele Identifier: CA686712340

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1390989767
• gnomAD v3: 12-25206414-TTTTGTC-T
• gnomAD v4: 12-25206414-TTTTGTC-T
• MyVariant Identifiers: chr12:g.25359349_25359354del (hg19) ; chr12:g.25206415_25206420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206418_25206423del , CM000674.2:g.25206418_25206423del	GRCh38
NC_000012.11:g.25359352_25359357del , CM000674.1:g.25359352_25359357del	GRCh37
NC_000012.10:g.25250619_25250624del	NCBI36
NG_007524.1:g.49501_49506del
NG_007524.2:g.49584_49589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3375_*3380del (KRAS)	ENSP00000508921.1:n.*3375_*3380del
ENST00000686877.1:c.*3913_*3918del (KRAS)	ENSP00000510431.1:n.*3913_*3918del
ENST00000687356.1:c.*3640_*3645del (KRAS)	ENSP00000510511.1:n.*3640_*3645del
ENST00000690406.1:c.3745_3750del (KRAS)
ENST00000692768.1:c.*3375_*3380del (KRAS)	ENSP00000510254.1:n.*3375_*3380del
ENST00000693229.1:c.*3375_*3380del (KRAS)	ENSP00000509223.1:n.*3375_*3380del
ENST00000256078.10:c.*3496_*3501del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3496_*3501del
ENST00000311936.8:c.*3375_*3380del (KRAS) MANE Select	ENSP00000308495.3:n.*3375_*3380del
ENST00000553788.6:c.51+2411_51+2416del (ETFRF1)	ENSP00000451938.2:n.51+2411_51+2416del
ENST00000311936.7:c.*3375_*3380del (KRAS)	ENSP00000308495.3:n.*3375_*3380del
ENST00000553788.5:c.45+2411_45+2416del (ETFRF1)	ENSP00000451938.1:n.45+2411_45+2416del
NM_004985.4:c.*3375_*3380del (KRAS)	NP_004976.2:n.*3375_*3380del
NM_033360.3:c.*3496_*3501del (KRAS)	NP_203524.1:n.*3496_*3501del
XM_011520653.1:c.*3375_*3380del (KRAS)	XP_011518955.1:n.*3375_*3380del
XM_011520653.3:c.*3375_*3380del (KRAS)	XP_011518955.1:n.*3375_*3380del
NM_001369786.1:c.*3496_*3501del (KRAS)	NP_001356715.1:n.*3496_*3501del
NM_001369787.1:c.*3375_*3380del (KRAS)	NP_001356716.1:n.*3375_*3380del
NM_004985.5:c.*3375_*3380del (KRAS) MANE Select	NP_004976.2:n.*3375_*3380del
NM_033360.4:c.*3496_*3501del (KRAS) MANE Plus Clinical	NP_203524.1:n.*3496_*3501del