Canonical Allele Identifier: CA162270282

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93462276C>T , CM000669.2:g.93462276C>T	GRCh38
NC_000007.13:g.93091588C>T , CM000669.1:g.93091588C>T	GRCh37
NC_000007.12:g.92929524C>T	NCBI36
NG_013005.1:g.117455G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001742.4:c.522-1329G>A MANE Select	NP_001733.1:n.522-1329G>A
ENST00000426151.7:c.522-1329G>A MANE Select	ENSP00000389295.1:n.522-1329G>A
NM_001164737.1:c.576-166G>A	NP_001158209.1:n.576-166G>A
NM_001164737.2:c.522-166G>A	NP_001158209.2:n.522-166G>A
NM_001164737.3:c.522-166G>A	NP_001158209.2:n.522-166G>A
NM_001164738.1:c.522-1329G>A	NP_001158210.1:n.522-1329G>A
NM_001164738.2:c.522-1329G>A	NP_001158210.1:n.522-1329G>A
NM_001742.3:c.522-1329G>A	NP_001733.1:n.522-1329G>A
ENST00000359558.6:c.576-166G>A	ENSP00000352561.2:n.576-166G>A
ENST00000360249.8:c.*32-1329G>A	ENSP00000353385.5:n.*32-1329G>A
ENST00000394441.5:c.522-1329G>A	ENSP00000377959.1:n.522-1329G>A
ENST00000415529.2:c.522-1329G>A	ENSP00000413179.1:n.522-1329G>A
ENST00000421592.5:c.522-166G>A	ENSP00000399552.1:n.522-166G>A
ENST00000423724.5:c.522-166G>A	ENSP00000391369.1:n.522-166G>A
ENST00000426151.5:c.522-1329G>A	ENSP00000389295.1:n.522-1329G>A
ENST00000649521.1:c.522-166G>A	ENSP00000497687.1:n.522-166G>A