Canonical Allele Identifier: CA456486060

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426503-A-G
• MyVariant Identifiers: chr7:g.93055815A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426503A>G , CM000669.2:g.93426503A>G	GRCh38
NC_000007.13:g.93055815A>G , CM000669.1:g.93055815A>G	GRCh37
NC_000007.12:g.92893751A>G	NCBI36
NG_013005.1:g.153228T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1278T>C MANE Select	ENSP00000389295.1:p.Ala426=
ENST00000649521.1:c.1326T>C	ENSP00000497687.1:p.Ala442=
ENST00000359558.6:c.1380T>C	ENSP00000352561.2:p.Ala460=
ENST00000360249.8:c.*788T>C	ENSP00000353385.5:n.*788T>C
ENST00000394441.5:c.1278T>C	ENSP00000377959.1:p.Ala426=
ENST00000415529.2:c.1328T>C	ENSP00000413179.1:n.1328T>C
ENST00000421592.5:c.1326T>C	ENSP00000399552.1:p.Ala442=
ENST00000423724.5:c.1376T>C	ENSP00000391369.1:n.1376T>C
ENST00000426151.5:c.1278T>C	ENSP00000389295.1:p.Ala426=
NM_001164737.1:c.1380T>C	NP_001158209.1:p.Ala460=
NM_001164738.1:c.1278T>C	NP_001158210.1:p.Ala426=
NM_001742.3:c.1278T>C	NP_001733.1:p.Ala426=
NM_001164737.2:c.1326T>C	NP_001158209.2:p.Ala442=
NM_001742.4:c.1278T>C MANE Select	NP_001733.1:p.Ala426=
NM_001164737.3:c.1326T>C	NP_001158209.2:p.Ala442=
NM_001164738.2:c.1278T>C	NP_001158210.1:p.Ala426=