Canonical Allele Identifier: CA1726312526

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426539G= , CM000669.2:g.93426539G=	GRCh38
NC_000007.13:g.93055851G= , CM000669.1:g.93055851G=	GRCh37
NC_000007.12:g.92893787G=	NCBI36
NG_013005.1:g.153192C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1242C= MANE Select	ENSP00000389295.1:p.Asn414=
ENST00000649521.1:c.1290C=	ENSP00000497687.1:p.Asn430=
ENST00000359558.6:c.1344C=	ENSP00000352561.2:p.Asn448=
ENST00000360249.8:c.*752C=	ENSP00000353385.5:n.*752C=
ENST00000394441.5:c.1242C=	ENSP00000377959.1:p.Asn414=
ENST00000415529.2:c.1292C=	ENSP00000413179.1:n.1292C=
ENST00000421592.5:c.1290C=	ENSP00000399552.1:p.Asn430=
ENST00000423724.5:c.1340C=	ENSP00000391369.1:n.1340C=
ENST00000426151.5:c.1242C=	ENSP00000389295.1:p.Asn414=
NM_001164737.1:c.1344C=	NP_001158209.1:p.Asn448=
NM_001164738.1:c.1242C=	NP_001158210.1:p.Asn414=
NM_001742.3:c.1242C=	NP_001733.1:p.Asn414=
NM_001164737.2:c.1290C=	NP_001158209.2:p.Asn430=
NM_001742.4:c.1242C= MANE Select	NP_001733.1:p.Asn414=
NM_001164737.3:c.1290C=	NP_001158209.2:p.Asn430=
NM_001164738.2:c.1242C=	NP_001158210.1:p.Asn414=