Canonical Allele Identifier: CA2578940302

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426347-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426347G>A , CM000669.2:g.93426347G>A	GRCh38
NC_000007.13:g.93055659G>A , CM000669.1:g.93055659G>A	GRCh37
NC_000007.12:g.92893595G>A	NCBI36
NG_013005.1:g.153384C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*9C>T MANE Select	ENSP00000389295.1:n.*9C>T
ENST00000649521.1:c.*9C>T	ENSP00000497687.1:n.*9C>T
ENST00000359558.6:c.*9C>T	ENSP00000352561.2:n.*9C>T
ENST00000360249.8:c.*944C>T	ENSP00000353385.5:n.*944C>T
ENST00000394441.5:c.*9C>T	ENSP00000377959.1:n.*9C>T
ENST00000421592.5:c.*9C>T	ENSP00000399552.1:n.*9C>T
ENST00000426151.5:c.*9C>T	ENSP00000389295.1:n.*9C>T
NM_001164737.1:c.*9C>T	NP_001158209.1:n.*9C>T
NM_001164738.1:c.*9C>T	NP_001158210.1:n.*9C>T
NM_001742.3:c.*9C>T	NP_001733.1:n.*9C>T
NM_001164737.2:c.*9C>T	NP_001158209.2:n.*9C>T
NM_001742.4:c.*9C>T MANE Select	NP_001733.1:n.*9C>T
NM_001164737.3:c.*9C>T	NP_001158209.2:n.*9C>T
NM_001164738.2:c.*9C>T	NP_001158210.1:n.*9C>T