Canonical Allele Identifier: CA368214708

Gene: CALCR

Linked Data

• MyVariant Identifiers: chr7:g.93055852T>G (hg19) ; chr7:g.93426540T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426540T>G , CM000669.2:g.93426540T>G	GRCh38
NC_000007.13:g.93055852T>G , CM000669.1:g.93055852T>G	GRCh37
NC_000007.12:g.92893788T>G	NCBI36
NG_013005.1:g.153191A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1241A>C MANE Select	ENSP00000389295.1:p.Asn414Thr
ENST00000649521.1:c.1289A>C	ENSP00000497687.1:p.Asn430Thr
ENST00000359558.6:c.1343A>C	ENSP00000352561.2:p.Asn448Thr
ENST00000360249.8:c.*751A>C	ENSP00000353385.5:n.*751A>C
ENST00000394441.5:c.1241A>C	ENSP00000377959.1:p.Asn414Thr
ENST00000415529.2:c.1291A>C	ENSP00000413179.1:n.1291A>C
ENST00000421592.5:c.1289A>C	ENSP00000399552.1:p.Asn430Thr
ENST00000423724.5:c.1339A>C	ENSP00000391369.1:n.1339A>C
ENST00000426151.5:c.1241A>C	ENSP00000389295.1:p.Asn414Thr
NM_001164737.1:c.1343A>C	NP_001158209.1:p.Asn448Thr
NM_001164738.1:c.1241A>C	NP_001158210.1:p.Asn414Thr
NM_001742.3:c.1241A>C	NP_001733.1:p.Asn414Thr
NM_001164737.2:c.1289A>C	NP_001158209.2:p.Asn430Thr
NM_001742.4:c.1241A>C MANE Select	NP_001733.1:p.Asn414Thr
NM_001164737.3:c.1289A>C	NP_001158209.2:p.Asn430Thr
NM_001164738.2:c.1241A>C	NP_001158210.1:p.Asn414Thr