Canonical Allele Identifier: CA61843489

Gene: CALCRL CALCRL-AS1

Linked Data

• dbSNP Id: rs779906834
• MyVariant Identifiers: chr2:g.188258821C>T (hg19) ; chr2:g.187394094C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.187394094C>T , CM000664.2:g.187394094C>T	GRCh38
NC_000002.11:g.188258821C>T , CM000664.1:g.188258821C>T	GRCh37
NC_000002.10:g.187967066C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392370.8:c.-292-6338G>A (CALCRL) MANE Select	ENSP00000376177.3:n.-292-6338G>A
ENST00000392370.7:c.-292-6338G>A (CALCRL)	ENSP00000376177.3:n.-292-6338G>A
ENST00000409998.5:c.-292-6338G>A (CALCRL)	ENSP00000386972.1:n.-292-6338G>A
ENST00000410068.5:c.-127-6338G>A (CALCRL)	ENSP00000387190.1:n.-127-6338G>A
ENST00000410102.5:c.-264-6338G>A (CALCRL)	ENSP00000386599.1:n.-264-6338G>A
ENST00000447403.5:c.-127-6338G>A (CALCRL)	ENSP00000415626.1:n.-127-6338G>A
ENST00000461244.5:n.479-6338G>A (CALCRL)
ENST00000474212.5:n.342-6338G>A (CALCRL)
ENST00000485973.1:n.216-6338G>A (CALCRL)
NM_001271751.1:c.-127-6338G>A (CALCRL)	NP_001258680.1:n.-127-6338G>A
NM_005795.5:c.-292-6338G>A (CALCRL)	NP_005786.1:n.-292-6338G>A
XM_005246231.2:c.-259-6338G>A (CALCRL)	XP_005246288.2:n.-259-6338G>A
XM_005246232.2:c.-259-6338G>A (CALCRL)	XP_005246289.2:n.-259-6338G>A
XM_005246234.2:c.-94-6338G>A (CALCRL)	XP_005246291.2:n.-94-6338G>A
XM_005246231.3:c.-259-6338G>A (CALCRL)	XP_005246288.2:n.-259-6338G>A
XM_005246232.3:c.-259-6338G>A (CALCRL)	XP_005246289.2:n.-259-6338G>A
XM_005246234.4:c.-94-6338G>A (CALCRL)	XP_005246291.2:n.-94-6338G>A
XM_017003151.2:c.-94-6338G>A (CALCRL)	XP_016858640.1:n.-94-6338G>A
XR_001739823.1:n.3420-105412C>T (CALCRL-AS1)
NM_005795.6:c.-292-6338G>A (CALCRL) MANE Select	NP_005786.1:n.-292-6338G>A
NM_001271751.2:c.-127-6338G>A (CALCRL)	NP_001258680.1:n.-127-6338G>A
NM_001369434.1:c.-292-6338G>A (CALCRL)	NP_001356363.1:n.-292-6338G>A
NM_001369435.1:c.-127-6338G>A (CALCRL)	NP_001356364.1:n.-127-6338G>A