Canonical Allele Identifier: CA1155329188

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445993_15445997delinsCTCAT , CM000663.2:g.15445993_15445997delinsCTCAT	GRCh38
NC_000001.10:g.15772488_15772492delinsCTCAT , CM000663.1:g.15772488_15772492delinsCTCAT	GRCh37
NC_000001.9:g.15645075_15645079delinsCTCAT	NCBI36
NG_009253.1:g.12551_12555delinsCTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+244_792+248delinsCTCAT MANE Select	ENSP00000365116.4:n.792+244_792+248delinsCTCAT
ENST00000375943.6:c.*246+244_*246+248delinsCTCAT	ENSP00000365110.2:n.*246+244_*246+248delinsCTCAT
ENST00000375949.4:c.792+244_792+248delinsCTCAT	ENSP00000365116.4:n.792+244_792+248delinsCTCAT
ENST00000483406.1:n.556+244_556+248delinsCTCAT
NM_007272.2:c.792+244_792+248delinsCTCAT	NP_009203.2:n.792+244_792+248delinsCTCAT
XM_011540550.1:c.646+244_646+248delinsCTCAT	XP_011538852.1:n.646+244_646+248delinsCTCAT
NM_007272.3:c.792+244_792+248delinsCTCAT MANE Select	NP_009203.2:n.792+244_792+248delinsCTCAT