Canonical Allele Identifier: CA372469226

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810744G>A (hg19) ; chr8:g.143728574G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728574G>A , CM000670.2:g.143728574G>A	GRCh38
NC_000008.10:g.144810744G>A , CM000670.1:g.144810744G>A	GRCh37
NC_000008.9:g.144882732G>A	NCBI36
NG_016652.1:g.10171C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.887C>T MANE Select	ENSP00000373565.3:p.Ala296Val
ENST00000650760.1:c.1490C>T	ENSP00000499217.1:p.Ala497Val
ENST00000388913.3:c.887C>T	ENSP00000373565.3:p.Ala296Val
ENST00000395103.2:c.67C>T
NM_198488.3:c.887C>T	NP_940890.3:p.Ala296Val
XM_005250887.2:c.944C>T	XP_005250944.1:p.Ala315Val
XM_005250888.2:c.905C>T	XP_005250945.1:p.Ala302Val
XM_005250889.2:c.887C>T	XP_005250946.1:p.Ala296Val
XM_011516980.1:c.1208C>T	XP_011515282.1:p.Ala403Val
XM_011516981.1:c.1055C>T	XP_011515283.1:p.Ala352Val
XM_005250887.3:c.944C>T	XP_005250944.1:p.Ala315Val
XM_005250888.3:c.905C>T	XP_005250945.1:p.Ala302Val
XM_005250889.3:c.887C>T	XP_005250946.1:p.Ala296Val
XM_011516980.2:c.1490C>T	XP_011515282.2:p.Ala497Val
XM_011516981.2:c.1055C>T	XP_011515283.1:p.Ala352Val
XM_024447131.1:c.887C>T	XP_024302899.1:p.Ala296Val
NM_198488.4:c.887C>T	NP_940890.3:p.Ala296Val
NM_198488.5:c.887C>T MANE Select	NP_940890.4:p.Ala296Val