Canonical Allele Identifier: CA2499629151

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426517-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426521dup , CM000669.2:g.93426521dup	GRCh38
NC_000007.13:g.93055833dup , CM000669.1:g.93055833dup	GRCh37
NC_000007.12:g.92893769dup	NCBI36
NG_013005.1:g.153213dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1263dup MANE Select	ENSP00000389295.1:p.Ser422LeufsTer29
ENST00000649521.1:c.1311dup	ENSP00000497687.1:p.Ser438LeufsTer29
ENST00000359558.6:c.1365dup	ENSP00000352561.2:p.Ser456LeufsTer29
ENST00000360249.8:c.*773dup	ENSP00000353385.5:n.*773dup
ENST00000394441.5:c.1263dup	ENSP00000377959.1:p.Ser422LeufsTer29
ENST00000415529.2:c.1313dup	ENSP00000413179.1:n.1313dup
ENST00000421592.5:c.1311dup	ENSP00000399552.1:p.Ser438LeufsTer29
ENST00000423724.5:c.1361dup	ENSP00000391369.1:n.1361dup
ENST00000426151.5:c.1263dup	ENSP00000389295.1:p.Ser422LeufsTer29
NM_001164737.1:c.1365dup	NP_001158209.1:p.Ser456LeufsTer29
NM_001164738.1:c.1263dup	NP_001158210.1:p.Ser422LeufsTer29
NM_001742.3:c.1263dup	NP_001733.1:p.Ser422LeufsTer29
NM_001164737.2:c.1311dup	NP_001158209.2:p.Ser438LeufsTer29
NM_001742.4:c.1263dup MANE Select	NP_001733.1:p.Ser422LeufsTer29
NM_001164737.3:c.1311dup	NP_001158209.2:p.Ser438LeufsTer29
NM_001164738.2:c.1263dup	NP_001158210.1:p.Ser422LeufsTer29