Canonical Allele Identifier: CA1726312568

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426637_93426638delinsTC , CM000669.2:g.93426637_93426638delinsTC	GRCh38
NC_000007.13:g.93055949_93055950delinsTC , CM000669.1:g.93055949_93055950delinsTC	GRCh37
NC_000007.12:g.92893885_92893886delinsTC	NCBI36
NG_013005.1:g.153093_153094delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1192-49_1192-48delinsGA MANE Select	ENSP00000389295.1:n.1192-49_1192-48delinsGA
ENST00000649521.1:c.1240-49_1240-48delinsGA	ENSP00000497687.1:n.1240-49_1240-48delinsGA
ENST00000359558.6:c.1294-49_1294-48delinsGA	ENSP00000352561.2:n.1294-49_1294-48delinsGA
ENST00000360249.8:c.*702-49_*702-48delinsGA	ENSP00000353385.5:n.*702-49_*702-48delinsGA
ENST00000394441.5:c.1192-49_1192-48delinsGA	ENSP00000377959.1:n.1192-49_1192-48delinsGA
ENST00000415529.2:c.1242-49_1242-48delinsGA	ENSP00000413179.1:n.1242-49_1242-48delinsGA
ENST00000421592.5:c.1240-49_1240-48delinsGA	ENSP00000399552.1:n.1240-49_1240-48delinsGA
ENST00000423724.5:c.1290-49_1290-48delinsGA	ENSP00000391369.1:n.1290-49_1290-48delinsGA
ENST00000426151.5:c.1192-49_1192-48delinsGA	ENSP00000389295.1:n.1192-49_1192-48delinsGA
NM_001164737.1:c.1294-49_1294-48delinsGA	NP_001158209.1:n.1294-49_1294-48delinsGA
NM_001164738.1:c.1192-49_1192-48delinsGA	NP_001158210.1:n.1192-49_1192-48delinsGA
NM_001742.3:c.1192-49_1192-48delinsGA	NP_001733.1:n.1192-49_1192-48delinsGA
NM_001164737.2:c.1240-49_1240-48delinsGA	NP_001158209.2:n.1240-49_1240-48delinsGA
NM_001742.4:c.1192-49_1192-48delinsGA MANE Select	NP_001733.1:n.1192-49_1192-48delinsGA
NM_001164737.3:c.1240-49_1240-48delinsGA	NP_001158209.2:n.1240-49_1240-48delinsGA
NM_001164738.2:c.1192-49_1192-48delinsGA	NP_001158210.1:n.1192-49_1192-48delinsGA