Canonical Allele Identifier: CA2022880946

Gene: KRAS ETFRF1

Linked Data

• dbSNP Id: rs1951136669

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.25206163_25206164del , CM000674.2:g.25206163_25206164del	GRCh38
NC_000012.11:g.25359097_25359098del , CM000674.1:g.25359097_25359098del	GRCh37
NC_000012.10:g.25250364_25250365del	NCBI36
NG_007524.1:g.49757_49758del
NG_007524.2:g.49840_49841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685328.1:c.*3631_*3632del (KRAS)	ENSP00000508921.1:n.*3631_*3632del
ENST00000686877.1:c.*4169_*4170del (KRAS)	ENSP00000510431.1:n.*4169_*4170del
ENST00000687356.1:c.*3896_*3897del (KRAS)	ENSP00000510511.1:n.*3896_*3897del
ENST00000690406.1:c.4001_4002del (KRAS)
ENST00000692768.1:c.*3631_*3632del (KRAS)	ENSP00000510254.1:n.*3631_*3632del
ENST00000693229.1:c.*3631_*3632del (KRAS)	ENSP00000509223.1:n.*3631_*3632del
ENST00000256078.10:c.*3752_*3753del (KRAS) MANE Plus Clinical	ENSP00000256078.5:n.*3752_*3753del
ENST00000311936.8:c.*3631_*3632del (KRAS) MANE Select	ENSP00000308495.3:n.*3631_*3632del
ENST00000553788.6:c.51+2156_51+2157del (ETFRF1)	ENSP00000451938.2:n.51+2156_51+2157del
ENST00000311936.7:c.*3631_*3632del (KRAS)	ENSP00000308495.3:n.*3631_*3632del
ENST00000553788.5:c.45+2156_45+2157del (ETFRF1)	ENSP00000451938.1:n.45+2156_45+2157del
NM_004985.4:c.*3631_*3632del (KRAS)	NP_004976.2:n.*3631_*3632del
NM_033360.3:c.*3752_*3753del (KRAS)	NP_203524.1:n.*3752_*3753del
XM_011520653.1:c.*3631_*3632del (KRAS)	XP_011518955.1:n.*3631_*3632del
XM_011520653.3:c.*3631_*3632del (KRAS)	XP_011518955.1:n.*3631_*3632del
NM_001369786.1:c.*3752_*3753del (KRAS)	NP_001356715.1:n.*3752_*3753del
NM_001369787.1:c.*3631_*3632del (KRAS)	NP_001356716.1:n.*3631_*3632del
NM_004985.5:c.*3631_*3632del (KRAS) MANE Select	NP_004976.2:n.*3631_*3632del
NM_033360.4:c.*3752_*3753del (KRAS) MANE Plus Clinical	NP_203524.1:n.*3752_*3753del