Canonical Allele Identifier: CA2056072865

Gene: FGD6

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95096472T>G , CM000674.2:g.95096472T>G	GRCh38
NC_000012.11:g.95490248T>G , CM000674.1:g.95490248T>G	GRCh37
NC_000012.10:g.94014379T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343958.9:c.3498-1778A>C MANE Select	ENSP00000344446.4:n.3498-1778A>C
ENST00000343958.8:c.3498-1778A>C	ENSP00000344446.4:n.3498-1778A>C
ENST00000451107.3:c.*893-1778A>C	ENSP00000408291.3:n.*893-1778A>C
ENST00000546711.5:c.3498-1778A>C	ENSP00000450342.1:n.3498-1778A>C
ENST00000549499.1:c.3498-1778A>C	ENSP00000449005.1:n.3498-1778A>C
ENST00000551521.5:c.486-1778A>C	ENSP00000450240.1:n.486-1778A>C
NM_018351.3:c.3498-1778A>C	NP_060821.3:n.3498-1778A>C
XR_002957422.1:n.318-6691T>G
NM_018351.4:c.3498-1778A>C MANE Select	NP_060821.3:n.3498-1778A>C