Canonical Allele Identifier: CA576707023

Gene: CALCR

Linked Data

• dbSNP Id: rs1398282371
• gnomAD v2: 7-93055905-G-GAAAAA
• MyVariant Identifiers: chr7:g.93055905_93055906insAAAAA (hg19) ; chr7:g.93426593_93426594insAAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426595_93426596insAAAAA , CM000669.2:g.93426595_93426596insAAAAA	GRCh38
NC_000007.13:g.93055907_93055908insAAAAA , CM000669.1:g.93055907_93055908insAAAAA	GRCh37
NC_000007.12:g.92893843_92893844insAAAAA	NCBI36
NG_013005.1:g.153137_153138insTTTTT

Transcript Alleles

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