Canonical Allele Identifier: CA1726312540

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426571G= , CM000669.2:g.93426571G=	GRCh38
NC_000007.13:g.93055883G= , CM000669.1:g.93055883G=	GRCh37
NC_000007.12:g.92893819G=	NCBI36
NG_013005.1:g.153160C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1210C= MANE Select	ENSP00000389295.1:p.Arg404=
ENST00000649521.1:c.1258C=	ENSP00000497687.1:p.Arg420=
ENST00000359558.6:c.1312C=	ENSP00000352561.2:p.Arg438=
ENST00000360249.8:c.*720C=	ENSP00000353385.5:n.*720C=
ENST00000394441.5:c.1210C=	ENSP00000377959.1:p.Arg404=
ENST00000415529.2:c.1260C=	ENSP00000413179.1:n.1260C=
ENST00000421592.5:c.1258C=	ENSP00000399552.1:p.Arg420=
ENST00000423724.5:c.1308C=	ENSP00000391369.1:n.1308C=
ENST00000426151.5:c.1210C=	ENSP00000389295.1:p.Arg404=
NM_001164737.1:c.1312C=	NP_001158209.1:p.Arg438=
NM_001164738.1:c.1210C=	NP_001158210.1:p.Arg404=
NM_001742.3:c.1210C=	NP_001733.1:p.Arg404=
NM_001164737.2:c.1258C=	NP_001158209.2:p.Arg420=
NM_001742.4:c.1210C= MANE Select	NP_001733.1:p.Arg404=
NM_001164737.3:c.1258C=	NP_001158209.2:p.Arg420=
NM_001164738.2:c.1210C=	NP_001158210.1:p.Arg404=