Canonical Allele Identifier: CA368214602

Gene: CALCR

Linked Data

• MyVariant Identifiers: chr7:g.93055820A>C (hg19) ; chr7:g.93426508A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426508A>C , CM000669.2:g.93426508A>C	GRCh38
NC_000007.13:g.93055820A>C , CM000669.1:g.93055820A>C	GRCh37
NC_000007.12:g.92893756A>C	NCBI36
NG_013005.1:g.153223T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1273T>G MANE Select	ENSP00000389295.1:p.Ser425Ala
ENST00000649521.1:c.1321T>G	ENSP00000497687.1:p.Ser441Ala
ENST00000359558.6:c.1375T>G	ENSP00000352561.2:p.Ser459Ala
ENST00000360249.8:c.*783T>G	ENSP00000353385.5:n.*783T>G
ENST00000394441.5:c.1273T>G	ENSP00000377959.1:p.Ser425Ala
ENST00000415529.2:c.1323T>G	ENSP00000413179.1:n.1323T>G
ENST00000421592.5:c.1321T>G	ENSP00000399552.1:p.Ser441Ala
ENST00000423724.5:c.1371T>G	ENSP00000391369.1:n.1371T>G
ENST00000426151.5:c.1273T>G	ENSP00000389295.1:p.Ser425Ala
NM_001164737.1:c.1375T>G	NP_001158209.1:p.Ser459Ala
NM_001164738.1:c.1273T>G	NP_001158210.1:p.Ser425Ala
NM_001742.3:c.1273T>G	NP_001733.1:p.Ser425Ala
NM_001164737.2:c.1321T>G	NP_001158209.2:p.Ser441Ala
NM_001742.4:c.1273T>G MANE Select	NP_001733.1:p.Ser425Ala
NM_001164737.3:c.1321T>G	NP_001158209.2:p.Ser441Ala
NM_001164738.2:c.1273T>G	NP_001158210.1:p.Ser425Ala