Canonical Allele Identifier: CA162272769

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93472679T>C , CM000669.2:g.93472679T>C	GRCh38
NC_000007.13:g.93101991T>C , CM000669.1:g.93101991T>C	GRCh37
NC_000007.12:g.92939927T>C	NCBI36
NG_013005.1:g.107052A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001742.4:c.317-192A>G MANE Select	NP_001733.1:n.317-192A>G
ENST00000426151.7:c.317-192A>G MANE Select	ENSP00000389295.1:n.317-192A>G
NM_001164737.1:c.371-192A>G	NP_001158209.1:n.371-192A>G
NM_001164737.2:c.317-192A>G	NP_001158209.2:n.317-192A>G
NM_001164737.3:c.317-192A>G	NP_001158209.2:n.317-192A>G
NM_001164738.1:c.317-192A>G	NP_001158210.1:n.317-192A>G
NM_001164738.2:c.317-192A>G	NP_001158210.1:n.317-192A>G
NM_001742.3:c.317-192A>G	NP_001733.1:n.317-192A>G
ENST00000359558.6:c.371-192A>G	ENSP00000352561.2:n.371-192A>G
ENST00000360249.8:c.317-192A>G	ENSP00000353385.5:n.317-192A>G
ENST00000394441.5:c.317-192A>G	ENSP00000377959.1:n.317-192A>G
ENST00000415529.2:c.317-192A>G	ENSP00000413179.1:n.317-192A>G
ENST00000421592.5:c.317-192A>G	ENSP00000399552.1:n.317-192A>G
ENST00000423724.5:c.317-192A>G	ENSP00000391369.1:n.317-192A>G
ENST00000426151.5:c.317-192A>G	ENSP00000389295.1:n.317-192A>G
ENST00000649521.1:c.317-192A>G	ENSP00000497687.1:n.317-192A>G