Canonical Allele Identifier: CA372469280

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728587-C-A
• MyVariant Identifiers: chr8:g.144810757C>A (hg19) ; chr8:g.143728587C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728587C>A , CM000670.2:g.143728587C>A	GRCh38
NC_000008.10:g.144810757C>A , CM000670.1:g.144810757C>A	GRCh37
NC_000008.9:g.144882745C>A	NCBI36
NG_016652.1:g.10158G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.874G>T MANE Select	ENSP00000373565.3:p.Ala292Ser
ENST00000650760.1:c.1477G>T	ENSP00000499217.1:p.Ala493Ser
ENST00000388913.3:c.874G>T	ENSP00000373565.3:p.Ala292Ser
ENST00000395103.2:c.54G>T
NM_198488.3:c.874G>T	NP_940890.3:p.Ala292Ser
XM_005250887.2:c.931G>T	XP_005250944.1:p.Ala311Ser
XM_005250888.2:c.892G>T	XP_005250945.1:p.Ala298Ser
XM_005250889.2:c.874G>T	XP_005250946.1:p.Ala292Ser
XM_011516980.1:c.1195G>T	XP_011515282.1:p.Ala399Ser
XM_011516981.1:c.1042G>T	XP_011515283.1:p.Ala348Ser
XM_005250887.3:c.931G>T	XP_005250944.1:p.Ala311Ser
XM_005250888.3:c.892G>T	XP_005250945.1:p.Ala298Ser
XM_005250889.3:c.874G>T	XP_005250946.1:p.Ala292Ser
XM_011516980.2:c.1477G>T	XP_011515282.2:p.Ala493Ser
XM_011516981.2:c.1042G>T	XP_011515283.1:p.Ala348Ser
XM_024447131.1:c.874G>T	XP_024302899.1:p.Ala292Ser
NM_198488.4:c.874G>T	NP_940890.3:p.Ala292Ser
NM_198488.5:c.874G>T MANE Select	NP_940890.4:p.Ala292Ser