Canonical Allele Identifier: CA1726312477

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426471T= , CM000669.2:g.93426471T=	GRCh38
NC_000007.13:g.93055783T= , CM000669.1:g.93055783T=	GRCh37
NC_000007.12:g.92893719T=	NCBI36
NG_013005.1:g.153260A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1310A= MANE Select	ENSP00000389295.1:p.Asp437=
ENST00000649521.1:c.1358A=	ENSP00000497687.1:p.Asp453=
ENST00000359558.6:c.1412A=	ENSP00000352561.2:p.Asp471=
ENST00000360249.8:c.*820A=	ENSP00000353385.5:n.*820A=
ENST00000394441.5:c.1310A=	ENSP00000377959.1:p.Asp437=
ENST00000415529.2:c.1360A=	ENSP00000413179.1:n.1360A=
ENST00000421592.5:c.1358A=	ENSP00000399552.1:p.Asp453=
ENST00000423724.5:c.1408A=	ENSP00000391369.1:n.1408A=
ENST00000426151.5:c.1310A=	ENSP00000389295.1:p.Asp437=
NM_001164737.1:c.1412A=	NP_001158209.1:p.Asp471=
NM_001164738.1:c.1310A=	NP_001158210.1:p.Asp437=
NM_001742.3:c.1310A=	NP_001733.1:p.Asp437=
NM_001164737.2:c.1358A=	NP_001158209.2:p.Asp453=
NM_001742.4:c.1310A= MANE Select	NP_001733.1:p.Asp437=
NM_001164737.3:c.1358A=	NP_001158209.2:p.Asp453=
NM_001164738.2:c.1310A=	NP_001158210.1:p.Asp437=