Canonical Allele Identifier: CA12475680

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93444060T>G , CM000669.2:g.93444060T>G	GRCh38
NC_000007.13:g.93073372T>G , CM000669.1:g.93073372T>G	GRCh37
NC_000007.12:g.92911308T>G	NCBI36
NG_013005.1:g.135671A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001742.4:c.649-303A>C MANE Select	NP_001733.1:n.649-303A>C
ENST00000426151.7:c.649-303A>C MANE Select	ENSP00000389295.1:n.649-303A>C
NM_001164737.1:c.751-303A>C	NP_001158209.1:n.751-303A>C
NM_001164737.2:c.697-303A>C	NP_001158209.2:n.697-303A>C
NM_001164737.3:c.697-303A>C	NP_001158209.2:n.697-303A>C
NM_001164738.1:c.649-303A>C	NP_001158210.1:n.649-303A>C
NM_001164738.2:c.649-303A>C	NP_001158210.1:n.649-303A>C
NM_001742.3:c.649-303A>C	NP_001733.1:n.649-303A>C
ENST00000359558.6:c.751-303A>C	ENSP00000352561.2:n.751-303A>C
ENST00000360249.8:c.*159-303A>C	ENSP00000353385.5:n.*159-303A>C
ENST00000394441.5:c.649-303A>C	ENSP00000377959.1:n.649-303A>C
ENST00000415529.2:c.649-303A>C	ENSP00000413179.1:n.649-303A>C
ENST00000421592.5:c.697-303A>C	ENSP00000399552.1:n.697-303A>C
ENST00000423724.5:c.697-303A>C	ENSP00000391369.1:n.697-303A>C
ENST00000426151.5:c.649-303A>C	ENSP00000389295.1:n.649-303A>C
ENST00000649521.1:c.697-303A>C	ENSP00000497687.1:n.697-303A>C