Canonical Allele Identifier: CA368214750

Gene: CALCR

Linked Data

• MyVariant Identifiers: chr7:g.93055862T>C (hg19) ; chr7:g.93426550T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426550T>C , CM000669.2:g.93426550T>C	GRCh38
NC_000007.13:g.93055862T>C , CM000669.1:g.93055862T>C	GRCh37
NC_000007.12:g.92893798T>C	NCBI36
NG_013005.1:g.153181A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1231A>G MANE Select	ENSP00000389295.1:p.Ile411Val
ENST00000649521.1:c.1279A>G	ENSP00000497687.1:p.Ile427Val
ENST00000359558.6:c.1333A>G	ENSP00000352561.2:p.Ile445Val
ENST00000360249.8:c.*741A>G	ENSP00000353385.5:n.*741A>G
ENST00000394441.5:c.1231A>G	ENSP00000377959.1:p.Ile411Val
ENST00000415529.2:c.1281A>G	ENSP00000413179.1:n.1281A>G
ENST00000421592.5:c.1279A>G	ENSP00000399552.1:p.Ile427Val
ENST00000423724.5:c.1329A>G	ENSP00000391369.1:n.1329A>G
ENST00000426151.5:c.1231A>G	ENSP00000389295.1:p.Ile411Val
NM_001164737.1:c.1333A>G	NP_001158209.1:p.Ile445Val
NM_001164738.1:c.1231A>G	NP_001158210.1:p.Ile411Val
NM_001742.3:c.1231A>G	NP_001733.1:p.Ile411Val
NM_001164737.2:c.1279A>G	NP_001158209.2:p.Ile427Val
NM_001742.4:c.1231A>G MANE Select	NP_001733.1:p.Ile411Val
NM_001164737.3:c.1279A>G	NP_001158209.2:p.Ile427Val
NM_001164738.2:c.1231A>G	NP_001158210.1:p.Ile411Val