Canonical Allele Identifier: CA463519961

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810719C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728549C>A , CM000670.2:g.143728549C>A	GRCh38
NC_000008.10:g.144810719C>A , CM000670.1:g.144810719C>A	GRCh37
NC_000008.9:g.144882707C>A	NCBI36
NG_016652.1:g.10196G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.912G>T MANE Select	ENSP00000373565.3:p.Gly304=
ENST00000650760.1:c.1515G>T	ENSP00000499217.1:p.Gly505=
ENST00000388913.3:c.912G>T	ENSP00000373565.3:p.Gly304=
ENST00000395103.2:c.92G>T
NM_198488.3:c.912G>T	NP_940890.3:p.Gly304=
XM_005250887.2:c.969G>T	XP_005250944.1:p.Gly323=
XM_005250888.2:c.930G>T	XP_005250945.1:p.Gly310=
XM_005250889.2:c.912G>T	XP_005250946.1:p.Gly304=
XM_011516980.1:c.1233G>T	XP_011515282.1:p.Gly411=
XM_011516981.1:c.1080G>T	XP_011515283.1:p.Gly360=
XM_005250887.3:c.969G>T	XP_005250944.1:p.Gly323=
XM_005250888.3:c.930G>T	XP_005250945.1:p.Gly310=
XM_005250889.3:c.912G>T	XP_005250946.1:p.Gly304=
XM_011516980.2:c.1515G>T	XP_011515282.2:p.Gly505=
XM_011516981.2:c.1080G>T	XP_011515283.1:p.Gly360=
XM_024447131.1:c.912G>T	XP_024302899.1:p.Gly304=
NM_198488.4:c.912G>T	NP_940890.3:p.Gly304=
NM_198488.5:c.912G>T MANE Select	NP_940890.4:p.Gly304=