Canonical Allele Identifier: CA4345506

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93460821C>T , CM000669.2:g.93460821C>T	GRCh38
NC_000007.13:g.93090133C>T , CM000669.1:g.93090133C>T	GRCh37
NC_000007.12:g.92928069C>T	NCBI36
NG_013005.1:g.118910G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.648G>A MANE Select	ENSP00000389295.1:p.Pro216=
ENST00000649521.1:c.696G>A	ENSP00000497687.1:p.Pro232=
ENST00000359558.6:c.750G>A	ENSP00000352561.2:p.Pro250=
ENST00000360249.8:c.*158G>A	ENSP00000353385.5:n.*158G>A
ENST00000394441.5:c.648G>A	ENSP00000377959.1:p.Pro216=
ENST00000415529.2:c.648G>A	ENSP00000413179.1:p.Pro216=
ENST00000421592.5:c.696G>A	ENSP00000399552.1:p.Pro232=
ENST00000423724.5:c.696G>A	ENSP00000391369.1:p.Pro232=
ENST00000426151.5:c.648G>A	ENSP00000389295.1:p.Pro216=
NM_001164737.1:c.750G>A	NP_001158209.1:p.Pro250=
NM_001164738.1:c.648G>A	NP_001158210.1:p.Pro216=
NM_001742.3:c.648G>A	NP_001733.1:p.Pro216=
NM_001164737.2:c.696G>A	NP_001158209.2:p.Pro232=
NM_001742.4:c.648G>A MANE Select	NP_001733.1:p.Pro216=
NM_001164737.3:c.696G>A	NP_001158209.2:p.Pro232=
NM_001164738.2:c.648G>A	NP_001158210.1:p.Pro216=