Canonical Allele Identifier: CA368214811

Gene: CALCR

Linked Data

• COSMIC: COSM6178988 ; COSM6178989
• MyVariant Identifiers: chr7:g.93055889C>A (hg19) ; chr7:g.93426577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426577C>A , CM000669.2:g.93426577C>A	GRCh38
NC_000007.13:g.93055889C>A , CM000669.1:g.93055889C>A	GRCh37
NC_000007.12:g.92893825C>A	NCBI36
NG_013005.1:g.153154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1204G>T MANE Select	ENSP00000389295.1:p.Val402Leu
ENST00000649521.1:c.1252G>T	ENSP00000497687.1:p.Val418Leu
ENST00000359558.6:c.1306G>T	ENSP00000352561.2:p.Val436Leu
ENST00000360249.8:c.*714G>T	ENSP00000353385.5:n.*714G>T
ENST00000394441.5:c.1204G>T	ENSP00000377959.1:p.Val402Leu
ENST00000415529.2:c.1254G>T	ENSP00000413179.1:n.1254G>T
ENST00000421592.5:c.1252G>T	ENSP00000399552.1:p.Val418Leu
ENST00000423724.5:c.1302G>T	ENSP00000391369.1:n.1302G>T
ENST00000426151.5:c.1204G>T	ENSP00000389295.1:p.Val402Leu
NM_001164737.1:c.1306G>T	NP_001158209.1:p.Val436Leu
NM_001164738.1:c.1204G>T	NP_001158210.1:p.Val402Leu
NM_001742.3:c.1204G>T	NP_001733.1:p.Val402Leu
NM_001164737.2:c.1252G>T	NP_001158209.2:p.Val418Leu
NM_001742.4:c.1204G>T MANE Select	NP_001733.1:p.Val402Leu
NM_001164737.3:c.1252G>T	NP_001158209.2:p.Val418Leu
NM_001164738.2:c.1204G>T	NP_001158210.1:p.Val402Leu