Canonical Allele Identifier: CA2578940339

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426531del , CM000669.2:g.93426531del	GRCh38
NC_000007.13:g.93055843del , CM000669.1:g.93055843del	GRCh37
NC_000007.12:g.92893779del	NCBI36
NG_013005.1:g.153204del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1254del MANE Select	ENSP00000389295.1:p.Arg419GlyfsTer29
ENST00000649521.1:c.1302del	ENSP00000497687.1:p.Arg435GlyfsTer29
ENST00000359558.6:c.1356del	ENSP00000352561.2:p.Arg453GlyfsTer29
ENST00000360249.8:c.*764del	ENSP00000353385.5:n.*764del
ENST00000394441.5:c.1254del	ENSP00000377959.1:p.Arg419GlyfsTer29
ENST00000415529.2:c.1304del	ENSP00000413179.1:n.1304del
ENST00000421592.5:c.1302del	ENSP00000399552.1:p.Arg435GlyfsTer29
ENST00000423724.5:c.1352del	ENSP00000391369.1:n.1352del
ENST00000426151.5:c.1254del	ENSP00000389295.1:p.Arg419GlyfsTer29
NM_001164737.1:c.1356del	NP_001158209.1:p.Arg453GlyfsTer29
NM_001164738.1:c.1254del	NP_001158210.1:p.Arg419GlyfsTer29
NM_001742.3:c.1254del	NP_001733.1:p.Arg419GlyfsTer29
NM_001164737.2:c.1302del	NP_001158209.2:p.Arg435GlyfsTer29
NM_001742.4:c.1254del MANE Select	NP_001733.1:p.Arg419GlyfsTer29
NM_001164737.3:c.1302del	NP_001158209.2:p.Arg435GlyfsTer29
NM_001164738.2:c.1254del	NP_001158210.1:p.Arg419GlyfsTer29