Canonical Allele Identifier: CA372468837

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728440-G-A
• MyVariant Identifiers: chr8:g.144810610G>A (hg19) ; chr8:g.143728440G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728440G>A , CM000670.2:g.143728440G>A	GRCh38
NC_000008.10:g.144810610G>A , CM000670.1:g.144810610G>A	GRCh37
NC_000008.9:g.144882598G>A	NCBI36
NG_016652.1:g.10305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.1021C>T MANE Select	ENSP00000373565.3:p.Pro341Ser
ENST00000650760.1:c.1624C>T	ENSP00000499217.1:p.Pro542Ser
ENST00000388913.3:c.1021C>T	ENSP00000373565.3:p.Pro341Ser
ENST00000395103.2:c.201C>T
NM_198488.3:c.1021C>T	NP_940890.3:p.Pro341Ser
XM_005250887.2:c.1078C>T	XP_005250944.1:p.Pro360Ser
XM_005250888.2:c.1039C>T	XP_005250945.1:p.Pro347Ser
XM_005250889.2:c.1021C>T	XP_005250946.1:p.Pro341Ser
XM_011516980.1:c.1342C>T	XP_011515282.1:p.Pro448Ser
XM_011516981.1:c.1189C>T	XP_011515283.1:p.Pro397Ser
XM_005250887.3:c.1078C>T	XP_005250944.1:p.Pro360Ser
XM_005250888.3:c.1039C>T	XP_005250945.1:p.Pro347Ser
XM_005250889.3:c.1021C>T	XP_005250946.1:p.Pro341Ser
XM_011516980.2:c.1624C>T	XP_011515282.2:p.Pro542Ser
XM_011516981.2:c.1189C>T	XP_011515283.1:p.Pro397Ser
XM_024447131.1:c.1021C>T	XP_024302899.1:p.Pro341Ser
NM_198488.4:c.1021C>T	NP_940890.3:p.Pro341Ser
NM_198488.5:c.1021C>T MANE Select	NP_940890.4:p.Pro341Ser