Canonical Allele Identifier: CA1726312531

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426555A= , CM000669.2:g.93426555A=	GRCh38
NC_000007.13:g.93055867A= , CM000669.1:g.93055867A=	GRCh37
NC_000007.12:g.92893803A=	NCBI36
NG_013005.1:g.153176T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1226T= MANE Select	ENSP00000389295.1:p.Phe409=
ENST00000649521.1:c.1274T=	ENSP00000497687.1:p.Phe425=
ENST00000359558.6:c.1328T=	ENSP00000352561.2:p.Phe443=
ENST00000360249.8:c.*736T=	ENSP00000353385.5:n.*736T=
ENST00000394441.5:c.1226T=	ENSP00000377959.1:p.Phe409=
ENST00000415529.2:c.1276T=	ENSP00000413179.1:n.1276T=
ENST00000421592.5:c.1274T=	ENSP00000399552.1:p.Phe425=
ENST00000423724.5:c.1324T=	ENSP00000391369.1:n.1324T=
ENST00000426151.5:c.1226T=	ENSP00000389295.1:p.Phe409=
NM_001164737.1:c.1328T=	NP_001158209.1:p.Phe443=
NM_001164738.1:c.1226T=	NP_001158210.1:p.Phe409=
NM_001742.3:c.1226T=	NP_001733.1:p.Phe409=
NM_001164737.2:c.1274T=	NP_001158209.2:p.Phe425=
NM_001742.4:c.1226T= MANE Select	NP_001733.1:p.Phe409=
NM_001164737.3:c.1274T=	NP_001158209.2:p.Phe425=
NM_001164738.2:c.1226T=	NP_001158210.1:p.Phe409=