Canonical Allele Identifier: CA2738526844

Gene: ARAF

Linked Data

• dbSNP Id: rs2147905703

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566785G>A , CM000685.2:g.47566785G>A	GRCh38
NC_000023.10:g.47426184G>A , CM000685.1:g.47426184G>A	GRCh37
NC_000023.9:g.47311128G>A	NCBI36
NG_016339.1:g.10669G>A
NG_016339.2:g.10669G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.699+5G>A MANE Select	ENSP00000366244.4:n.699+5G>A
ENST00000290277.10:c.708+5G>A	ENSP00000290277.7:n.708+5G>A
ENST00000377045.8:c.699+5G>A	ENSP00000366244.4:n.699+5G>A
NM_001256196.1:c.708+5G>A	NP_001243125.1:n.708+5G>A
NM_001654.4:c.699+5G>A	NP_001645.1:n.699+5G>A
XM_006724529.1:c.714+5G>A	XP_006724592.1:n.714+5G>A
XM_011543906.1:c.714+5G>A	XP_011542208.1:n.714+5G>A
XM_011543907.1:c.714+5G>A	XP_011542209.1:n.714+5G>A
XM_011543908.1:c.699+5G>A	XP_011542210.1:n.699+5G>A
XM_011543909.1:c.42+5G>A	XP_011542211.1:n.42+5G>A
XM_006724529.3:c.714+5G>A	XP_006724592.1:n.714+5G>A
XM_011543906.3:c.714+5G>A	XP_011542208.1:n.714+5G>A
XM_011543908.3:c.699+5G>A	XP_011542210.1:n.699+5G>A
XM_011543909.3:c.42+5G>A	XP_011542211.1:n.42+5G>A
NM_001654.5:c.699+5G>A MANE Select	NP_001645.1:n.699+5G>A
NM_001256196.2:c.708+5G>A	NP_001243125.1:n.708+5G>A