Canonical Allele Identifier: CA456486057

Gene: CALCR

Linked Data

• MyVariant Identifiers: chr7:g.93055812G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426500G>T , CM000669.2:g.93426500G>T	GRCh38
NC_000007.13:g.93055812G>T , CM000669.1:g.93055812G>T	GRCh37
NC_000007.12:g.92893748G>T	NCBI36
NG_013005.1:g.153231C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1281C>A MANE Select	ENSP00000389295.1:p.Arg427=
ENST00000649521.1:c.1329C>A	ENSP00000497687.1:p.Arg443=
ENST00000359558.6:c.1383C>A	ENSP00000352561.2:p.Arg461=
ENST00000360249.8:c.*791C>A	ENSP00000353385.5:n.*791C>A
ENST00000394441.5:c.1281C>A	ENSP00000377959.1:p.Arg427=
ENST00000415529.2:c.1331C>A	ENSP00000413179.1:n.1331C>A
ENST00000421592.5:c.1329C>A	ENSP00000399552.1:p.Arg443=
ENST00000423724.5:c.1379C>A	ENSP00000391369.1:n.1379C>A
ENST00000426151.5:c.1281C>A	ENSP00000389295.1:p.Arg427=
NM_001164737.1:c.1383C>A	NP_001158209.1:p.Arg461=
NM_001164738.1:c.1281C>A	NP_001158210.1:p.Arg427=
NM_001742.3:c.1281C>A	NP_001733.1:p.Arg427=
NM_001164737.2:c.1329C>A	NP_001158209.2:p.Arg443=
NM_001742.4:c.1281C>A MANE Select	NP_001733.1:p.Arg427=
NM_001164737.3:c.1329C>A	NP_001158209.2:p.Arg443=
NM_001164738.2:c.1281C>A	NP_001158210.1:p.Arg427=