Canonical Allele Identifier: CA843978877

Gene: CALCR

Linked Data

• dbSNP Id: rs1301697966
• MyVariant Identifiers: chr7:g.93056092A>G (hg19) ; chr7:g.93426780A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426780A>G , CM000669.2:g.93426780A>G	GRCh38
NC_000007.13:g.93056092A>G , CM000669.1:g.93056092A>G	GRCh37
NC_000007.12:g.92894028A>G	NCBI36
NG_013005.1:g.152951T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1192-191T>C MANE Select	ENSP00000389295.1:n.1192-191T>C
ENST00000649521.1:c.1240-191T>C	ENSP00000497687.1:n.1240-191T>C
ENST00000359558.6:c.1294-191T>C	ENSP00000352561.2:n.1294-191T>C
ENST00000360249.8:c.*702-191T>C	ENSP00000353385.5:n.*702-191T>C
ENST00000394441.5:c.1192-191T>C	ENSP00000377959.1:n.1192-191T>C
ENST00000415529.2:c.1242-191T>C	ENSP00000413179.1:n.1242-191T>C
ENST00000421592.5:c.1240-191T>C	ENSP00000399552.1:n.1240-191T>C
ENST00000423724.5:c.1290-191T>C	ENSP00000391369.1:n.1290-191T>C
ENST00000426151.5:c.1192-191T>C	ENSP00000389295.1:n.1192-191T>C
NM_001164737.1:c.1294-191T>C	NP_001158209.1:n.1294-191T>C
NM_001164738.1:c.1192-191T>C	NP_001158210.1:n.1192-191T>C
NM_001742.3:c.1192-191T>C	NP_001733.1:n.1192-191T>C
NM_001164737.2:c.1240-191T>C	NP_001158209.2:n.1240-191T>C
NM_001742.4:c.1192-191T>C MANE Select	NP_001733.1:n.1192-191T>C
NM_001164737.3:c.1240-191T>C	NP_001158209.2:n.1240-191T>C
NM_001164738.2:c.1192-191T>C	NP_001158210.1:n.1192-191T>C