Canonical Allele Identifier: CA1347296763

Gene: FGD5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.14858271G= , CM000665.2:g.14858271G=	GRCh38
NC_000003.11:g.14899778G= , CM000665.1:g.14899778G=	GRCh37
NC_000003.10:g.14874782G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_152536.4:c.2526-5857G= MANE Select	NP_689749.3:n.2526-5857G=
ENST00000285046.10:c.2526-5857G= MANE Select	ENSP00000285046.5:n.2526-5857G=
NM_001320276.1:c.2526-5857G=	NP_001307205.1:n.2526-5857G=
NM_001320276.2:c.2526-5857G=	NP_001307205.1:n.2526-5857G=
NM_152536.3:c.2526-5857G=	NP_689749.3:n.2526-5857G=
ENST00000285046.9:c.2526-5857G=	ENSP00000285046.5:n.2526-5857G=
ENST00000457774.1:c.166-5857G=
ENST00000543601.5:c.1803-5857G=	ENSP00000445949.1:n.1803-5857G=
XM_011533422.1:c.2526-5857G=	XP_011531724.1:n.2526-5857G=
XM_011533423.1:c.2526-5857G=	XP_011531725.1:n.2526-5857G=
XM_011533424.1:c.2526-5857G=	XP_011531726.1:n.2526-5857G=