Canonical Allele Identifier: CA372467816

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810369T>A (hg19) ; chr8:g.143728199T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728199T>A , CM000670.2:g.143728199T>A	GRCh38
NC_000008.10:g.144810369T>A , CM000670.1:g.144810369T>A	GRCh37
NC_000008.9:g.144882357T>A	NCBI36
NG_016652.1:g.10546A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.1262A>T MANE Select	ENSP00000373565.3:p.Glu421Val
ENST00000650760.1:c.1865A>T	ENSP00000499217.1:p.Glu622Val
ENST00000388913.3:c.1262A>T	ENSP00000373565.3:p.Glu421Val
ENST00000395103.2:c.442A>T
NM_198488.3:c.1262A>T	NP_940890.3:p.Glu421Val
XM_005250887.2:c.1319A>T	XP_005250944.1:p.Glu440Val
XM_005250888.2:c.1280A>T	XP_005250945.1:p.Glu427Val
XM_005250889.2:c.1262A>T	XP_005250946.1:p.Glu421Val
XM_011516980.1:c.1583A>T	XP_011515282.1:p.Glu528Val
XM_011516981.1:c.1430A>T	XP_011515283.1:p.Glu477Val
XM_005250887.3:c.1319A>T	XP_005250944.1:p.Glu440Val
XM_005250888.3:c.1280A>T	XP_005250945.1:p.Glu427Val
XM_005250889.3:c.1262A>T	XP_005250946.1:p.Glu421Val
XM_011516980.2:c.1865A>T	XP_011515282.2:p.Glu622Val
XM_011516981.2:c.1430A>T	XP_011515283.1:p.Glu477Val
XM_024447131.1:c.1262A>T	XP_024302899.1:p.Glu421Val
NM_198488.4:c.1262A>T	NP_940890.3:p.Glu421Val
NM_198488.5:c.1262A>T MANE Select	NP_940890.4:p.Glu421Val