Canonical Allele Identifier: CA1726312396

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426318G= , CM000669.2:g.93426318G=	GRCh38
NC_000007.13:g.93055630G= , CM000669.1:g.93055630G=	GRCh37
NC_000007.12:g.92893566G=	NCBI36
NG_013005.1:g.153413C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*38C= MANE Select	ENSP00000389295.1:n.*38C=
ENST00000649521.1:c.*38C=	ENSP00000497687.1:n.*38C=
ENST00000359558.6:c.*38C=	ENSP00000352561.2:n.*38C=
ENST00000360249.8:c.*973C=	ENSP00000353385.5:n.*973C=
ENST00000421592.5:c.*38C=	ENSP00000399552.1:n.*38C=
NM_001164737.1:c.*38C=	NP_001158209.1:n.*38C=
NM_001164738.1:c.*38C=	NP_001158210.1:n.*38C=
NM_001742.3:c.*38C=	NP_001733.1:n.*38C=
NM_001164737.2:c.*38C=	NP_001158209.2:n.*38C=
NM_001742.4:c.*38C= MANE Select	NP_001733.1:n.*38C=
NM_001164737.3:c.*38C=	NP_001158209.2:n.*38C=
NM_001164738.2:c.*38C=	NP_001158210.1:n.*38C=