Canonical Allele Identifier: CA1726312402

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426328T= , CM000669.2:g.93426328T=	GRCh38
NC_000007.13:g.93055640T= , CM000669.1:g.93055640T=	GRCh37
NC_000007.12:g.92893576T=	NCBI36
NG_013005.1:g.153403A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*28A= MANE Select	ENSP00000389295.1:n.*28A=
ENST00000649521.1:c.*28A=	ENSP00000497687.1:n.*28A=
ENST00000359558.6:c.*28A=	ENSP00000352561.2:n.*28A=
ENST00000360249.8:c.*963A=	ENSP00000353385.5:n.*963A=
ENST00000394441.5:c.*28A=	ENSP00000377959.1:n.*28A=
ENST00000421592.5:c.*28A=	ENSP00000399552.1:n.*28A=
ENST00000426151.5:c.*28A=	ENSP00000389295.1:n.*28A=
NM_001164737.1:c.*28A=	NP_001158209.1:n.*28A=
NM_001164738.1:c.*28A=	NP_001158210.1:n.*28A=
NM_001742.3:c.*28A=	NP_001733.1:n.*28A=
NM_001164737.2:c.*28A=	NP_001158209.2:n.*28A=
NM_001742.4:c.*28A= MANE Select	NP_001733.1:n.*28A=
NM_001164737.3:c.*28A=	NP_001158209.2:n.*28A=
NM_001164738.2:c.*28A=	NP_001158210.1:n.*28A=