Canonical Allele Identifier: CA1155329129

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445943_15445959delinsTATTCATTCACTCATGC , CM000663.2:g.15445943_15445959delinsTATTCATTCACTCATGC	GRCh38
NC_000001.10:g.15772438_15772454delinsTATTCATTCACTCATGC , CM000663.1:g.15772438_15772454delinsTATTCATTCACTCATGC	GRCh37
NC_000001.9:g.15645025_15645041delinsTATTCATTCACTCATGC	NCBI36
NG_009253.1:g.12501_12517delinsTATTCATTCACTCATGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+194_792+210delinsTATTCATTCACTCATGC MANE Select	ENSP00000365116.4:n.792+194_792+210delinsTATTCATTCACTCATGC
ENST00000375943.6:c.*246+194_*246+210delinsTATTCATTCACTCATGC	ENSP00000365110.2:n.*246+194_*246+210delinsTATTCATTCACTCATGC
ENST00000375949.4:c.792+194_792+210delinsTATTCATTCACTCATGC	ENSP00000365116.4:n.792+194_792+210delinsTATTCATTCACTCATGC
ENST00000483406.1:n.556+194_556+210delinsTATTCATTCACTCATGC
NM_007272.2:c.792+194_792+210delinsTATTCATTCACTCATGC	NP_009203.2:n.792+194_792+210delinsTATTCATTCACTCATGC
XM_011540550.1:c.646+194_646+210delinsTATTCATTCACTCATGC	XP_011538852.1:n.646+194_646+210delinsTATTCATTCACTCATGC
NM_007272.3:c.792+194_792+210delinsTATTCATTCACTCATGC MANE Select	NP_009203.2:n.792+194_792+210delinsTATTCATTCACTCATGC