Canonical Allele Identifier: CA372469165

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810727A>C (hg19) ; chr8:g.143728557A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728557A>C , CM000670.2:g.143728557A>C	GRCh38
NC_000008.10:g.144810727A>C , CM000670.1:g.144810727A>C	GRCh37
NC_000008.9:g.144882715A>C	NCBI36
NG_016652.1:g.10188T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.904T>G MANE Select	ENSP00000373565.3:p.Tyr302Asp
ENST00000650760.1:c.1507T>G	ENSP00000499217.1:p.Tyr503Asp
ENST00000388913.3:c.904T>G	ENSP00000373565.3:p.Tyr302Asp
ENST00000395103.2:c.84T>G
NM_198488.3:c.904T>G	NP_940890.3:p.Tyr302Asp
XM_005250887.2:c.961T>G	XP_005250944.1:p.Tyr321Asp
XM_005250888.2:c.922T>G	XP_005250945.1:p.Tyr308Asp
XM_005250889.2:c.904T>G	XP_005250946.1:p.Tyr302Asp
XM_011516980.1:c.1225T>G	XP_011515282.1:p.Tyr409Asp
XM_011516981.1:c.1072T>G	XP_011515283.1:p.Tyr358Asp
XM_005250887.3:c.961T>G	XP_005250944.1:p.Tyr321Asp
XM_005250888.3:c.922T>G	XP_005250945.1:p.Tyr308Asp
XM_005250889.3:c.904T>G	XP_005250946.1:p.Tyr302Asp
XM_011516980.2:c.1507T>G	XP_011515282.2:p.Tyr503Asp
XM_011516981.2:c.1072T>G	XP_011515283.1:p.Tyr358Asp
XM_024447131.1:c.904T>G	XP_024302899.1:p.Tyr302Asp
NM_198488.4:c.904T>G	NP_940890.3:p.Tyr302Asp
NM_198488.5:c.904T>G MANE Select	NP_940890.4:p.Tyr302Asp