Canonical Allele Identifier: CA576707022

Gene: CALCR

Linked Data

• dbSNP Id: rs1415265661
• gnomAD v2: 7-93055900-ACCTGG-A
• gnomAD v4: 7-93426588-ACCTGG-A
• MyVariant Identifiers: chr7:g.93055901_93055905del (hg19) ; chr7:g.93426589_93426593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426589_93426593del , CM000669.2:g.93426589_93426593del	GRCh38
NC_000007.13:g.93055901_93055905del , CM000669.1:g.93055901_93055905del	GRCh37
NC_000007.12:g.92893837_92893841del	NCBI36
NG_013005.1:g.153138_153142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1192-4_1192del
ENST00000649521.1:c.1240-4_1240del
ENST00000359558.6:c.1294-4_1294del
ENST00000360249.8:c.*702-4_*702del
ENST00000394441.5:c.1192-4_1192del
ENST00000415529.2:c.1242-4_1242del
ENST00000421592.5:c.1240-4_1240del
ENST00000423724.5:c.1290-4_1290del
ENST00000426151.5:c.1192-4_1192del
NM_001164737.1:c.1294-4_1294del
NM_001164738.1:c.1192-4_1192del
NM_001742.3:c.1192-4_1192del
NM_001164737.2:c.1240-4_1240del
NM_001742.4:c.1192-4_1192del
NM_001164737.3:c.1240-4_1240del
NM_001164738.2:c.1192-4_1192del