Canonical Allele Identifier: CA456486108

Gene: CALCR

Linked Data

• dbSNP Id: rs549002704
• MyVariant Identifiers: chr7:g.93055899G>C (hg19) ; chr7:g.93426587G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426587G>C , CM000669.2:g.93426587G>C	GRCh38
NC_000007.13:g.93055899G>C , CM000669.1:g.93055899G>C	GRCh37
NC_000007.12:g.92893835G>C	NCBI36
NG_013005.1:g.153144C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1194C>G MANE Select	ENSP00000389295.1:p.Val398=
ENST00000649521.1:c.1242C>G	ENSP00000497687.1:p.Val414=
ENST00000359558.6:c.1296C>G	ENSP00000352561.2:p.Val432=
ENST00000360249.8:c.*704C>G	ENSP00000353385.5:n.*704C>G
ENST00000394441.5:c.1194C>G	ENSP00000377959.1:p.Val398=
ENST00000415529.2:c.1244C>G	ENSP00000413179.1:n.1244C>G
ENST00000421592.5:c.1242C>G	ENSP00000399552.1:p.Val414=
ENST00000423724.5:c.1292C>G	ENSP00000391369.1:n.1292C>G
ENST00000426151.5:c.1194C>G	ENSP00000389295.1:p.Val398=
NM_001164737.1:c.1296C>G	NP_001158209.1:p.Val432=
NM_001164738.1:c.1194C>G	NP_001158210.1:p.Val398=
NM_001742.3:c.1194C>G	NP_001733.1:p.Val398=
NM_001164737.2:c.1242C>G	NP_001158209.2:p.Val414=
NM_001742.4:c.1194C>G MANE Select	NP_001733.1:p.Val398=
NM_001164737.3:c.1242C>G	NP_001158209.2:p.Val414=
NM_001164738.2:c.1194C>G	NP_001158210.1:p.Val398=