Canonical Allele Identifier: CA372468935

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728473-A-T
• MyVariant Identifiers: chr8:g.144810643A>T (hg19) ; chr8:g.143728473A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728473A>T , CM000670.2:g.143728473A>T	GRCh38
NC_000008.10:g.144810643A>T , CM000670.1:g.144810643A>T	GRCh37
NC_000008.9:g.144882631A>T	NCBI36
NG_016652.1:g.10272T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.988T>A MANE Select	ENSP00000373565.3:p.Phe330Ile
ENST00000650760.1:c.1591T>A	ENSP00000499217.1:p.Phe531Ile
ENST00000388913.3:c.988T>A	ENSP00000373565.3:p.Phe330Ile
ENST00000395103.2:c.168T>A
NM_198488.3:c.988T>A	NP_940890.3:p.Phe330Ile
XM_005250887.2:c.1045T>A	XP_005250944.1:p.Phe349Ile
XM_005250888.2:c.1006T>A	XP_005250945.1:p.Phe336Ile
XM_005250889.2:c.988T>A	XP_005250946.1:p.Phe330Ile
XM_011516980.1:c.1309T>A	XP_011515282.1:p.Phe437Ile
XM_011516981.1:c.1156T>A	XP_011515283.1:p.Phe386Ile
XM_005250887.3:c.1045T>A	XP_005250944.1:p.Phe349Ile
XM_005250888.3:c.1006T>A	XP_005250945.1:p.Phe336Ile
XM_005250889.3:c.988T>A	XP_005250946.1:p.Phe330Ile
XM_011516980.2:c.1591T>A	XP_011515282.2:p.Phe531Ile
XM_011516981.2:c.1156T>A	XP_011515283.1:p.Phe386Ile
XM_024447131.1:c.988T>A	XP_024302899.1:p.Phe330Ile
NM_198488.4:c.988T>A	NP_940890.3:p.Phe330Ile
NM_198488.5:c.988T>A MANE Select	NP_940890.4:p.Phe330Ile