Canonical Allele Identifier: CA2683748893

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426561-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426564dup , CM000669.2:g.93426564dup	GRCh38
NC_000007.13:g.93055876dup , CM000669.1:g.93055876dup	GRCh37
NC_000007.12:g.92893812dup	NCBI36
NG_013005.1:g.153169dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1219dup MANE Select	ENSP00000389295.1:p.Ala407GlyfsTer?
ENST00000649521.1:c.1267dup	ENSP00000497687.1:p.Ala423GlyfsTer?
ENST00000359558.6:c.1321dup	ENSP00000352561.2:p.Ala441GlyfsTer?
ENST00000360249.8:c.*729dup	ENSP00000353385.5:n.*729dup
ENST00000394441.5:c.1219dup	ENSP00000377959.1:p.Ala407GlyfsTer?
ENST00000415529.2:c.1269dup	ENSP00000413179.1:n.1269dup
ENST00000421592.5:c.1267dup	ENSP00000399552.1:p.Ala423GlyfsTer?
ENST00000423724.5:c.1317dup	ENSP00000391369.1:n.1317dup
ENST00000426151.5:c.1219dup	ENSP00000389295.1:p.Ala407GlyfsTer?
NM_001164737.1:c.1321dup	NP_001158209.1:p.Ala441GlyfsTer?
NM_001164738.1:c.1219dup	NP_001158210.1:p.Ala407GlyfsTer?
NM_001742.3:c.1219dup	NP_001733.1:p.Ala407GlyfsTer?
NM_001164737.2:c.1267dup	NP_001158209.2:p.Ala423GlyfsTer?
NM_001742.4:c.1219dup MANE Select	NP_001733.1:p.Ala407GlyfsTer?
NM_001164737.3:c.1267dup	NP_001158209.2:p.Ala423GlyfsTer?
NM_001164738.2:c.1219dup	NP_001158210.1:p.Ala407GlyfsTer?