Canonical Allele Identifier: CA2683748979

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426721-CTGTGTAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426722_93426728del , CM000669.2:g.93426722_93426728del	GRCh38
NC_000007.13:g.93056034_93056040del , CM000669.1:g.93056034_93056040del	GRCh37
NC_000007.12:g.92893970_92893976del	NCBI36
NG_013005.1:g.153003_153009del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1192-139_1192-133del MANE Select	ENSP00000389295.1:n.1192-139_1192-133del
ENST00000649521.1:c.1240-139_1240-133del	ENSP00000497687.1:n.1240-139_1240-133del
ENST00000359558.6:c.1294-139_1294-133del	ENSP00000352561.2:n.1294-139_1294-133del
ENST00000360249.8:c.*702-139_*702-133del	ENSP00000353385.5:n.*702-139_*702-133del
ENST00000394441.5:c.1192-139_1192-133del	ENSP00000377959.1:n.1192-139_1192-133del
ENST00000415529.2:c.1242-139_1242-133del	ENSP00000413179.1:n.1242-139_1242-133del
ENST00000421592.5:c.1240-139_1240-133del	ENSP00000399552.1:n.1240-139_1240-133del
ENST00000423724.5:c.1290-139_1290-133del	ENSP00000391369.1:n.1290-139_1290-133del
ENST00000426151.5:c.1192-139_1192-133del	ENSP00000389295.1:n.1192-139_1192-133del
NM_001164737.1:c.1294-139_1294-133del	NP_001158209.1:n.1294-139_1294-133del
NM_001164738.1:c.1192-139_1192-133del	NP_001158210.1:n.1192-139_1192-133del
NM_001742.3:c.1192-139_1192-133del	NP_001733.1:n.1192-139_1192-133del
NM_001164737.2:c.1240-139_1240-133del	NP_001158209.2:n.1240-139_1240-133del
NM_001742.4:c.1192-139_1192-133del MANE Select	NP_001733.1:n.1192-139_1192-133del
NM_001164737.3:c.1240-139_1240-133del	NP_001158209.2:n.1240-139_1240-133del
NM_001164738.2:c.1192-139_1192-133del	NP_001158210.1:n.1192-139_1192-133del