Canonical Allele Identifier: CA368214389

Gene: CALCR

Linked Data

• MyVariant Identifiers: chr7:g.93055761A>T (hg19) ; chr7:g.93426449A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426449A>T , CM000669.2:g.93426449A>T	GRCh38
NC_000007.13:g.93055761A>T , CM000669.1:g.93055761A>T	GRCh37
NC_000007.12:g.92893697A>T	NCBI36
NG_013005.1:g.153282T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426151.7:c.1332T>A MANE Select	ENSP00000389295.1:p.His444Gln
ENST00000649521.1:c.1380T>A	ENSP00000497687.1:p.His460Gln
ENST00000359558.6:c.1434T>A	ENSP00000352561.2:p.His478Gln
ENST00000360249.8:c.*842T>A	ENSP00000353385.5:n.*842T>A
ENST00000394441.5:c.1332T>A	ENSP00000377959.1:p.His444Gln
ENST00000415529.2:c.1382T>A	ENSP00000413179.1:n.1382T>A
ENST00000421592.5:c.1380T>A	ENSP00000399552.1:p.His460Gln
ENST00000423724.5:c.1430T>A	ENSP00000391369.1:n.1430T>A
ENST00000426151.5:c.1332T>A	ENSP00000389295.1:p.His444Gln
NM_001164737.1:c.1434T>A	NP_001158209.1:p.His478Gln
NM_001164738.1:c.1332T>A	NP_001158210.1:p.His444Gln
NM_001742.3:c.1332T>A	NP_001733.1:p.His444Gln
NM_001164737.2:c.1380T>A	NP_001158209.2:p.His460Gln
NM_001742.4:c.1332T>A MANE Select	NP_001733.1:p.His444Gln
NM_001164737.3:c.1380T>A	NP_001158209.2:p.His460Gln
NM_001164738.2:c.1332T>A	NP_001158210.1:p.His444Gln