Canonical Allele Identifier: CA372469159

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810726T>G (hg19) ; chr8:g.143728556T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728556T>G , CM000670.2:g.143728556T>G	GRCh38
NC_000008.10:g.144810726T>G , CM000670.1:g.144810726T>G	GRCh37
NC_000008.9:g.144882714T>G	NCBI36
NG_016652.1:g.10189A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.905A>C MANE Select	ENSP00000373565.3:p.Tyr302Ser
ENST00000650760.1:c.1508A>C	ENSP00000499217.1:p.Tyr503Ser
ENST00000388913.3:c.905A>C	ENSP00000373565.3:p.Tyr302Ser
ENST00000395103.2:c.85A>C
NM_198488.3:c.905A>C	NP_940890.3:p.Tyr302Ser
XM_005250887.2:c.962A>C	XP_005250944.1:p.Tyr321Ser
XM_005250888.2:c.923A>C	XP_005250945.1:p.Tyr308Ser
XM_005250889.2:c.905A>C	XP_005250946.1:p.Tyr302Ser
XM_011516980.1:c.1226A>C	XP_011515282.1:p.Tyr409Ser
XM_011516981.1:c.1073A>C	XP_011515283.1:p.Tyr358Ser
XM_005250887.3:c.962A>C	XP_005250944.1:p.Tyr321Ser
XM_005250888.3:c.923A>C	XP_005250945.1:p.Tyr308Ser
XM_005250889.3:c.905A>C	XP_005250946.1:p.Tyr302Ser
XM_011516980.2:c.1508A>C	XP_011515282.2:p.Tyr503Ser
XM_011516981.2:c.1073A>C	XP_011515283.1:p.Tyr358Ser
XM_024447131.1:c.905A>C	XP_024302899.1:p.Tyr302Ser
NM_198488.4:c.905A>C	NP_940890.3:p.Tyr302Ser
NM_198488.5:c.905A>C MANE Select	NP_940890.4:p.Tyr302Ser