Canonical Allele Identifier: CA4917571

Gene: FAM83H

Linked Data

• dbSNP Id: rs782465375
• ExAC: 8:144810767 G / A
• gnomAD v2: 8-144810767-G-A
• gnomAD v3: 8-143728597-G-A
• gnomAD v4: 8-143728597-G-A
• MyVariant Identifiers: chr8:g.144810767G>A (hg19) ; chr8:g.143728597G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728597G>A , CM000670.2:g.143728597G>A	GRCh38
NC_000008.10:g.144810767G>A , CM000670.1:g.144810767G>A	GRCh37
NC_000008.9:g.144882755G>A	NCBI36
NG_016652.1:g.10148C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.864C>T MANE Select	ENSP00000373565.3:p.Ala288=
ENST00000650760.1:c.1467C>T	ENSP00000499217.1:p.Ala489=
ENST00000388913.3:c.864C>T	ENSP00000373565.3:p.Ala288=
ENST00000395103.2:c.44C>T
NM_198488.3:c.864C>T	NP_940890.3:p.Ala288=
XM_005250887.2:c.921C>T	XP_005250944.1:p.Ala307=
XM_005250888.2:c.882C>T	XP_005250945.1:p.Ala294=
XM_005250889.2:c.864C>T	XP_005250946.1:p.Ala288=
XM_011516980.1:c.1185C>T	XP_011515282.1:p.Ala395=
XM_011516981.1:c.1032C>T	XP_011515283.1:p.Ala344=
XM_005250887.3:c.921C>T	XP_005250944.1:p.Ala307=
XM_005250888.3:c.882C>T	XP_005250945.1:p.Ala294=
XM_005250889.3:c.864C>T	XP_005250946.1:p.Ala288=
XM_011516980.2:c.1467C>T	XP_011515282.2:p.Ala489=
XM_011516981.2:c.1032C>T	XP_011515283.1:p.Ala344=
XM_024447131.1:c.864C>T	XP_024302899.1:p.Ala288=
NM_198488.4:c.864C>T	NP_940890.3:p.Ala288=
NM_198488.5:c.864C>T MANE Select	NP_940890.4:p.Ala288=