Canonical Allele Identifier: CA61836167

Gene: CALCRL CALCRL-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.187359330A>G , CM000664.2:g.187359330A>G	GRCh38
NC_000002.11:g.188224057A>G , CM000664.1:g.188224057A>G	GRCh37
NC_000002.10:g.187932302A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005795.6:c.782-58T>C (CALCRL) MANE Select	NP_005786.1:n.782-58T>C
ENST00000392370.8:c.782-58T>C (CALCRL) MANE Select	ENSP00000376177.3:n.782-58T>C
NM_001271751.1:c.782-58T>C (CALCRL)	NP_001258680.1:n.782-58T>C
NM_001271751.2:c.782-58T>C (CALCRL)	NP_001258680.1:n.782-58T>C
NM_001369434.1:c.782-58T>C (CALCRL)	NP_001356363.1:n.782-58T>C
NM_001369435.1:c.782-58T>C (CALCRL)	NP_001356364.1:n.782-58T>C
NM_005795.5:c.782-58T>C (CALCRL)	NP_005786.1:n.782-58T>C
ENST00000392370.7:c.782-58T>C (CALCRL)	ENSP00000376177.3:n.782-58T>C
ENST00000409998.5:c.782-58T>C (CALCRL)	ENSP00000386972.1:n.782-58T>C
ENST00000410068.5:c.782-58T>C (CALCRL)	ENSP00000387190.1:n.782-58T>C
XM_005246231.2:c.815-58T>C (CALCRL)	XP_005246288.2:n.815-58T>C
XM_005246231.3:c.815-58T>C (CALCRL)	XP_005246288.2:n.815-58T>C
XM_005246232.2:c.815-58T>C (CALCRL)	XP_005246289.2:n.815-58T>C
XM_005246232.3:c.815-58T>C (CALCRL)	XP_005246289.2:n.815-58T>C
XM_005246234.2:c.815-58T>C (CALCRL)	XP_005246291.2:n.815-58T>C
XM_005246234.4:c.815-58T>C (CALCRL)	XP_005246291.2:n.815-58T>C
XM_017003151.2:c.815-58T>C (CALCRL)	XP_016858640.1:n.815-58T>C
XR_001739823.1:n.3420-140176A>G (CALCRL-AS1)