Canonical Allele Identifier: CA1726312493

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426493C= , CM000669.2:g.93426493C=	GRCh38
NC_000007.13:g.93055805C= , CM000669.1:g.93055805C=	GRCh37
NC_000007.12:g.92893741C=	NCBI36
NG_013005.1:g.153238G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1288G= MANE Select	ENSP00000389295.1:p.Ala430=
ENST00000649521.1:c.1336G=	ENSP00000497687.1:p.Ala446=
ENST00000359558.6:c.1390G=	ENSP00000352561.2:p.Ala464=
ENST00000360249.8:c.*798G=	ENSP00000353385.5:n.*798G=
ENST00000394441.5:c.1288G=	ENSP00000377959.1:p.Ala430=
ENST00000415529.2:c.1338G=	ENSP00000413179.1:n.1338G=
ENST00000421592.5:c.1336G=	ENSP00000399552.1:p.Ala446=
ENST00000423724.5:c.1386G=	ENSP00000391369.1:n.1386G=
ENST00000426151.5:c.1288G=	ENSP00000389295.1:p.Ala430=
NM_001164737.1:c.1390G=	NP_001158209.1:p.Ala464=
NM_001164738.1:c.1288G=	NP_001158210.1:p.Ala430=
NM_001742.3:c.1288G=	NP_001733.1:p.Ala430=
NM_001164737.2:c.1336G=	NP_001158209.2:p.Ala446=
NM_001742.4:c.1288G= MANE Select	NP_001733.1:p.Ala430=
NM_001164737.3:c.1336G=	NP_001158209.2:p.Ala446=
NM_001164738.2:c.1288G=	NP_001158210.1:p.Ala430=