Canonical Allele Identifier: CA177689

Gene: RAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12664125_12664126del , CM000665.2:g.12664125_12664126del	GRCh38
NC_000003.11:g.12705624_12705625del , CM000665.1:g.12705624_12705625del	GRCh37
NC_000003.10:g.12680624_12680625del	NCBI36
NG_007467.1:g.5057_5058del , LRG_413:g.5057_5058del

Transcript Alleles

HGVS	Amino-acid Change
NM_001354689.1:c.-337_-336del	NP_001341618.1:n.-337_-336del
NM_001354691.1:c.-560_-559del	NP_001341620.1:n.-560_-559del
NM_001354692.1:c.-467_-466del	NP_001341621.1:n.-467_-466del
NM_001354693.1:c.-337_-336del	NP_001341622.1:n.-337_-336del
NM_001354694.1:c.-467_-466del	NP_001341623.1:n.-467_-466del
NM_001354695.1:c.-467_-466del	NP_001341624.1:n.-467_-466del
NM_002880.3:c.-337_-336del , LRG_413t1:c.-337_-336del	NP_002871.1:n.-337_-336del
NR_148940.1:n.79_80del
NR_148941.1:n.79_80del
NR_148942.1:n.79_80del
ENST00000251849.8:c.-337_-336del	ENSP00000251849.4:n.-337_-336del
ENST00000442415.6:c.-337_-336del	ENSP00000401888.2:n.-337_-336del
ENST00000491290.2:n.41_42del
ENST00000684903.1:c.-337_-336del	ENSP00000508612.1:n.-337_-336del
ENST00000685348.1:c.-337_-336del	ENSP00000510285.1:n.-337_-336del
ENST00000686455.1:n.27_28del
ENST00000686479.1:n.35_36del
ENST00000687940.1:n.41_42del
ENST00000688543.1:c.-337_-336del	ENSP00000509612.1:n.-337_-336del
ENST00000689914.1:c.-337_-336del	ENSP00000509847.1:n.-337_-336del
ENST00000691396.1:c.-337_-336del	ENSP00000510712.1:n.-337_-336del
ENST00000692093.1:c.-430_-429del	ENSP00000509669.1:n.-430_-429del
ENST00000692311.1:n.37_38del
ENST00000692558.1:n.29_30del
XM_005265358.3:c.-467_-466del	XP_005265415.1:n.-467_-466del
XM_005265359.3:c.-467_-466del	XP_005265416.1:n.-467_-466del
XM_011533974.1:c.-430_-429del	XP_011532276.1:n.-430_-429del
XM_011533975.1:c.-560_-559del	XP_011532277.1:n.-560_-559del