Canonical Allele Identifier: CA1726312285

Gene: CALCR

Linked Data

• dbSNP Id: rs1799518071
• gnomAD v4: 7-93426013-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426013G>A , CM000669.2:g.93426013G>A	GRCh38
NC_000007.13:g.93055325G>A , CM000669.1:g.93055325G>A	GRCh37
NC_000007.12:g.92893261G>A	NCBI36
NG_013005.1:g.153718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*343C>T MANE Select	ENSP00000389295.1:n.*343C>T
ENST00000649521.1:c.*343C>T	ENSP00000497687.1:n.*343C>T
ENST00000359558.6:c.*343C>T	ENSP00000352561.2:n.*343C>T
ENST00000421592.5:c.*343C>T	ENSP00000399552.1:n.*343C>T
NM_001164737.1:c.*343C>T	NP_001158209.1:n.*343C>T
NM_001164738.1:c.*343C>T	NP_001158210.1:n.*343C>T
NM_001742.3:c.*343C>T	NP_001733.1:n.*343C>T
NM_001164737.2:c.*343C>T	NP_001158209.2:n.*343C>T
NM_001742.4:c.*343C>T MANE Select	NP_001733.1:n.*343C>T
NM_001164737.3:c.*343C>T	NP_001158209.2:n.*343C>T
NM_001164738.2:c.*343C>T	NP_001158210.1:n.*343C>T