Canonical Allele Identifier: CA2573939412

Gene: FCGR3A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161544770_161544781del , CM000663.2:g.161544770_161544781del	GRCh38
NC_000001.10:g.161514560_161514571del , CM000663.1:g.161514560_161514571del	GRCh37
NC_000001.9:g.159781184_159781195del	NCBI36
NG_009066.1:g.10845_10856del , LRG_60:g.10845_10856del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367967.8:c.499_510del	ENSP00000356944.3:p.Ser167_Tyr170del
ENST00000426740.8:c.496_507del	ENSP00000410180.3:p.Ser166_Tyr169del
ENST00000436743.7:c.499_510del	ENSP00000416607.1:p.Ser167_Tyr170del
ENST00000699395.1:c.499_510del	ENSP00000514356.1:p.Ser167_Tyr170del
ENST00000699396.1:c.499_510del	ENSP00000514357.1:p.Ser167_Tyr170del
ENST00000699397.1:c.499_510del	ENSP00000514358.1:p.Ser167_Tyr170del
ENST00000699398.1:c.499_510del	ENSP00000514359.1:p.Ser167_Tyr170del
ENST00000699399.1:c.448_459del	ENSP00000514360.1:p.Ser150_Tyr153del
ENST00000699400.1:c.496_507del	ENSP00000514361.1:p.Ser166_Tyr169del
ENST00000699401.1:c.499_510del	ENSP00000514362.1:p.Ser167_Tyr170del
ENST00000426740.7:c.496_507del	ENSP00000410180.3:p.Ser166_Tyr169del
ENST00000436743.6:c.499_510del	ENSP00000416607.1:p.Ser167_Tyr170del
ENST00000443193.6:c.499_510del MANE Select	ENSP00000392047.2:p.Ser167_Tyr170del
ENST00000367967.7:c.499_510del	ENSP00000356944.3:p.Ser167_Tyr170del
ENST00000367969.7:c.607_618del	ENSP00000356946.3:p.Ser203_Tyr206del
ENST00000426740.5:c.549_560del
ENST00000436743.5:c.499_510del	ENSP00000416607.1:p.Ser167_Tyr170del
ENST00000443193.5:c.499_510del	ENSP00000392047.2:p.Ser167_Tyr170del
NM_000569.6:c.607_618del	NP_000560.5:p.Ser203_Tyr206del
NM_001127592.1:c.604_615del	NP_001121064.1:p.Ser202_Tyr205del
NM_001127593.1:c.499_510del , LRG_60t1:c.499_510del	NP_001121065.1:p.Ser167_Tyr170del
NM_001127595.1:c.499_510del	NP_001121067.1:p.Ser167_Tyr170del
NM_001127596.1:c.496_507del	NP_001121068.1:p.Ser166_Tyr169del
XM_011509293.1:c.428-1580_428-1569del	XP_011507595.1:n.428-1580_428-1569del
NM_000569.7:c.814_825del	NP_000560.6:p.Ser272_Tyr275del
NM_001127592.2:c.811_822del	NP_001121064.2:p.Ser271_Tyr274del
NM_001329120.1:c.499_510del	NP_001316049.1:p.Ser167_Tyr170del
NM_001329122.1:c.635-1580_635-1569del	NP_001316051.1:n.635-1580_635-1569del
XM_024454064.1:c.496_507del	XP_024309832.1:p.Ser166_Tyr169del
NM_001127595.2:c.499_510del	NP_001121067.1:p.Ser167_Tyr170del
NM_001127596.2:c.496_507del	NP_001121068.1:p.Ser166_Tyr169del
NM_000569.8:c.499_510del MANE Select	NP_000560.7:p.Ser167_Tyr170del
NM_001329120.2:c.499_510del	NP_001316049.1:p.Ser167_Tyr170del
NM_001386450.1:c.496_507del	NP_001373379.1:p.Ser166_Tyr169del