Canonical Allele Identifier: CA2683748892

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426526-T-TC

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1254dup MANE Select	ENSP00000389295.1:p.Arg419GlufsTer?
ENST00000649521.1:c.1302dup	ENSP00000497687.1:p.Arg435GlufsTer?
ENST00000359558.6:c.1356dup	ENSP00000352561.2:p.Arg453GlufsTer?
ENST00000360249.8:c.*764dup	ENSP00000353385.5:n.*764dup
ENST00000394441.5:c.1254dup	ENSP00000377959.1:p.Arg419GlufsTer?
ENST00000415529.2:c.1304dup	ENSP00000413179.1:n.1304dup
ENST00000421592.5:c.1302dup	ENSP00000399552.1:p.Arg435GlufsTer?
ENST00000423724.5:c.1352dup	ENSP00000391369.1:n.1352dup
ENST00000426151.5:c.1254dup	ENSP00000389295.1:p.Arg419GlufsTer?
NM_001164737.1:c.1356dup	NP_001158209.1:p.Arg453GlufsTer?
NM_001164738.1:c.1254dup	NP_001158210.1:p.Arg419GlufsTer?
NM_001742.3:c.1254dup	NP_001733.1:p.Arg419GlufsTer?
NM_001164737.2:c.1302dup	NP_001158209.2:p.Arg435GlufsTer?
NM_001742.4:c.1254dup MANE Select	NP_001733.1:p.Arg419GlufsTer?
NM_001164737.3:c.1302dup	NP_001158209.2:p.Arg435GlufsTer?
NM_001164738.2:c.1254dup	NP_001158210.1:p.Arg419GlufsTer?