Canonical Allele Identifier: CA15492986

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93443359G>T , CM000669.2:g.93443359G>T	GRCh38
NC_000007.13:g.93072671G>T , CM000669.1:g.93072671G>T	GRCh37
NC_000007.12:g.92910607G>T	NCBI36
NG_013005.1:g.136372C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001742.4:c.802+245C>A MANE Select	NP_001733.1:n.802+245C>A
ENST00000426151.7:c.802+245C>A MANE Select	ENSP00000389295.1:n.802+245C>A
NM_001164737.1:c.904+245C>A	NP_001158209.1:n.904+245C>A
NM_001164737.2:c.850+245C>A	NP_001158209.2:n.850+245C>A
NM_001164737.3:c.850+245C>A	NP_001158209.2:n.850+245C>A
NM_001164738.1:c.802+245C>A	NP_001158210.1:n.802+245C>A
NM_001164738.2:c.802+245C>A	NP_001158210.1:n.802+245C>A
NM_001742.3:c.802+245C>A	NP_001733.1:n.802+245C>A
ENST00000359558.6:c.904+245C>A	ENSP00000352561.2:n.904+245C>A
ENST00000360249.8:c.*312+245C>A	ENSP00000353385.5:n.*312+245C>A
ENST00000394441.5:c.802+245C>A	ENSP00000377959.1:n.802+245C>A
ENST00000415529.2:c.802+245C>A	ENSP00000413179.1:n.802+245C>A
ENST00000421592.5:c.850+245C>A	ENSP00000399552.1:n.850+245C>A
ENST00000423724.5:c.850+245C>A	ENSP00000391369.1:n.850+245C>A
ENST00000426151.5:c.802+245C>A	ENSP00000389295.1:n.802+245C>A
ENST00000649521.1:c.850+245C>A	ENSP00000497687.1:n.850+245C>A