Canonical Allele Identifier: CA843978866

Gene: CALCR

Linked Data

• dbSNP Id: rs1331509897
• gnomAD v3: 7-93426750-A-AACTT
• gnomAD v4: 7-93426750-A-AACTT
• MyVariant Identifiers: chr7:g.93056062_93056063insACTT (hg19) ; chr7:g.93426750_93426751insACTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426751_93426754dup , CM000669.2:g.93426751_93426754dup	GRCh38
NC_000007.13:g.93056063_93056066dup , CM000669.1:g.93056063_93056066dup	GRCh37
NC_000007.12:g.92893999_92894002dup	NCBI36
NG_013005.1:g.152977_152980dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1192-165_1192-162dup MANE Select	ENSP00000389295.1:n.1192-165_1192-162dup
ENST00000649521.1:c.1240-165_1240-162dup	ENSP00000497687.1:n.1240-165_1240-162dup
ENST00000359558.6:c.1294-165_1294-162dup	ENSP00000352561.2:n.1294-165_1294-162dup
ENST00000360249.8:c.*702-165_*702-162dup	ENSP00000353385.5:n.*702-165_*702-162dup
ENST00000394441.5:c.1192-165_1192-162dup	ENSP00000377959.1:n.1192-165_1192-162dup
ENST00000415529.2:c.1242-165_1242-162dup	ENSP00000413179.1:n.1242-165_1242-162dup
ENST00000421592.5:c.1240-165_1240-162dup	ENSP00000399552.1:n.1240-165_1240-162dup
ENST00000423724.5:c.1290-165_1290-162dup	ENSP00000391369.1:n.1290-165_1290-162dup
ENST00000426151.5:c.1192-165_1192-162dup	ENSP00000389295.1:n.1192-165_1192-162dup
NM_001164737.1:c.1294-165_1294-162dup	NP_001158209.1:n.1294-165_1294-162dup
NM_001164738.1:c.1192-165_1192-162dup	NP_001158210.1:n.1192-165_1192-162dup
NM_001742.3:c.1192-165_1192-162dup	NP_001733.1:n.1192-165_1192-162dup
NM_001164737.2:c.1240-165_1240-162dup	NP_001158209.2:n.1240-165_1240-162dup
NM_001742.4:c.1192-165_1192-162dup MANE Select	NP_001733.1:n.1192-165_1192-162dup
NM_001164737.3:c.1240-165_1240-162dup	NP_001158209.2:n.1240-165_1240-162dup
NM_001164738.2:c.1192-165_1192-162dup	NP_001158210.1:n.1192-165_1192-162dup