Canonical Allele Identifier: CA2738527432

Gene: ARAF

Linked Data

• dbSNP Id: rs2147905858

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47566829G>T , CM000685.2:g.47566829G>T	GRCh38
NC_000023.10:g.47426228G>T , CM000685.1:g.47426228G>T	GRCh37
NC_000023.9:g.47311172G>T	NCBI36
NG_016339.1:g.10713G>T
NG_016339.2:g.10713G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377045.9:c.699+49G>T MANE Select	ENSP00000366244.4:n.699+49G>T
ENST00000290277.10:c.708+49G>T	ENSP00000290277.7:n.708+49G>T
ENST00000377045.8:c.699+49G>T	ENSP00000366244.4:n.699+49G>T
NM_001256196.1:c.708+49G>T	NP_001243125.1:n.708+49G>T
NM_001654.4:c.699+49G>T	NP_001645.1:n.699+49G>T
XM_006724529.1:c.714+49G>T	XP_006724592.1:n.714+49G>T
XM_011543906.1:c.714+49G>T	XP_011542208.1:n.714+49G>T
XM_011543907.1:c.714+49G>T	XP_011542209.1:n.714+49G>T
XM_011543908.1:c.699+49G>T	XP_011542210.1:n.699+49G>T
XM_011543909.1:c.42+49G>T	XP_011542211.1:n.42+49G>T
XM_006724529.3:c.714+49G>T	XP_006724592.1:n.714+49G>T
XM_011543906.3:c.714+49G>T	XP_011542208.1:n.714+49G>T
XM_011543908.3:c.699+49G>T	XP_011542210.1:n.699+49G>T
XM_011543909.3:c.42+49G>T	XP_011542211.1:n.42+49G>T
NM_001654.5:c.699+49G>T MANE Select	NP_001645.1:n.699+49G>T
NM_001256196.2:c.708+49G>T	NP_001243125.1:n.708+49G>T