Canonical Allele Identifier: CA162274570

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93479771T>A , CM000669.2:g.93479771T>A	GRCh38
NC_000007.13:g.93109083T>A , CM000669.1:g.93109083T>A	GRCh37
NC_000007.12:g.92947019T>A	NCBI36
NG_013005.1:g.99960A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001742.4:c.52-264A>T MANE Select	NP_001733.1:n.52-264A>T
ENST00000426151.7:c.52-264A>T MANE Select	ENSP00000389295.1:n.52-264A>T
NM_001164737.1:c.106-264A>T	NP_001158209.1:n.106-264A>T
NM_001164737.2:c.52-264A>T	NP_001158209.2:n.52-264A>T
NM_001164737.3:c.52-264A>T	NP_001158209.2:n.52-264A>T
NM_001164738.1:c.52-264A>T	NP_001158210.1:n.52-264A>T
NM_001164738.2:c.52-264A>T	NP_001158210.1:n.52-264A>T
NM_001742.3:c.52-264A>T	NP_001733.1:n.52-264A>T
ENST00000359558.6:c.106-264A>T	ENSP00000352561.2:n.106-264A>T
ENST00000360249.8:c.52-264A>T	ENSP00000353385.5:n.52-264A>T
ENST00000394441.5:c.52-264A>T	ENSP00000377959.1:n.52-264A>T
ENST00000415529.2:c.52-264A>T	ENSP00000413179.1:n.52-264A>T
ENST00000421592.5:c.52-264A>T	ENSP00000399552.1:n.52-264A>T
ENST00000423724.5:c.52-264A>T	ENSP00000391369.1:n.52-264A>T
ENST00000426151.5:c.52-264A>T	ENSP00000389295.1:n.52-264A>T
ENST00000649521.1:c.52-264A>T	ENSP00000497687.1:n.52-264A>T