Canonical Allele Identifier: CA463519780

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728492-A-G
• MyVariant Identifiers: chr8:g.144810662A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728492A>G , CM000670.2:g.143728492A>G	GRCh38
NC_000008.10:g.144810662A>G , CM000670.1:g.144810662A>G	GRCh37
NC_000008.9:g.144882650A>G	NCBI36
NG_016652.1:g.10253T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.969T>C MANE Select	ENSP00000373565.3:p.Pro323=
ENST00000650760.1:c.1572T>C	ENSP00000499217.1:p.Pro524=
ENST00000388913.3:c.969T>C	ENSP00000373565.3:p.Pro323=
ENST00000395103.2:c.149T>C
NM_198488.3:c.969T>C	NP_940890.3:p.Pro323=
XM_005250887.2:c.1026T>C	XP_005250944.1:p.Pro342=
XM_005250888.2:c.987T>C	XP_005250945.1:p.Pro329=
XM_005250889.2:c.969T>C	XP_005250946.1:p.Pro323=
XM_011516980.1:c.1290T>C	XP_011515282.1:p.Pro430=
XM_011516981.1:c.1137T>C	XP_011515283.1:p.Pro379=
XM_005250887.3:c.1026T>C	XP_005250944.1:p.Pro342=
XM_005250888.3:c.987T>C	XP_005250945.1:p.Pro329=
XM_005250889.3:c.969T>C	XP_005250946.1:p.Pro323=
XM_011516980.2:c.1572T>C	XP_011515282.2:p.Pro524=
XM_011516981.2:c.1137T>C	XP_011515283.1:p.Pro379=
XM_024447131.1:c.969T>C	XP_024302899.1:p.Pro323=
NM_198488.4:c.969T>C	NP_940890.3:p.Pro323=
NM_198488.5:c.969T>C MANE Select	NP_940890.4:p.Pro323=