Canonical Allele Identifier: CA1726312370

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426245_93426246delinsCT , CM000669.2:g.93426245_93426246delinsCT	GRCh38
NC_000007.13:g.93055557_93055558delinsCT , CM000669.1:g.93055557_93055558delinsCT	GRCh37
NC_000007.12:g.92893493_92893494delinsCT	NCBI36
NG_013005.1:g.153485_153486delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*110_*111delinsAG MANE Select	ENSP00000389295.1:n.*110_*111delinsAG
ENST00000649521.1:c.*110_*111delinsAG	ENSP00000497687.1:n.*110_*111delinsAG
ENST00000359558.6:c.*110_*111delinsAG	ENSP00000352561.2:n.*110_*111delinsAG
ENST00000421592.5:c.*110_*111delinsAG	ENSP00000399552.1:n.*110_*111delinsAG
NM_001164737.1:c.*110_*111delinsAG	NP_001158209.1:n.*110_*111delinsAG
NM_001164738.1:c.*110_*111delinsAG	NP_001158210.1:n.*110_*111delinsAG
NM_001742.3:c.*110_*111delinsAG	NP_001733.1:n.*110_*111delinsAG
NM_001164737.2:c.*110_*111delinsAG	NP_001158209.2:n.*110_*111delinsAG
NM_001742.4:c.*110_*111delinsAG MANE Select	NP_001733.1:n.*110_*111delinsAG
NM_001164737.3:c.*110_*111delinsAG	NP_001158209.2:n.*110_*111delinsAG
NM_001164738.2:c.*110_*111delinsAG	NP_001158210.1:n.*110_*111delinsAG