Canonical Allele Identifier: CA1140626879

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446004_15446017delinsATTCATTCATTCAT , CM000663.2:g.15446004_15446017delinsATTCATTCATTCAT	GRCh38
NC_000001.10:g.15772499_15772512delinsATTCATTCATTCAT , CM000663.1:g.15772499_15772512delinsATTCATTCATTCAT	GRCh37
NC_000001.9:g.15645086_15645099delinsATTCATTCATTCAT	NCBI36
NG_009253.1:g.12562_12575delinsATTCATTCATTCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+255_792+268delinsATTCATTCATTCAT MANE Select	ENSP00000365116.4:n.792+255_792+268delinsATTCATTCATTCAT
ENST00000375943.6:c.*246+255_*246+268delinsATTCATTCATTCAT	ENSP00000365110.2:n.*246+255_*246+268delinsATTCATTCATTCAT
ENST00000375949.4:c.792+255_792+268delinsATTCATTCATTCAT	ENSP00000365116.4:n.792+255_792+268delinsATTCATTCATTCAT
ENST00000483406.1:n.556+255_556+268delinsATTCATTCATTCAT
NM_007272.2:c.792+255_792+268delinsATTCATTCATTCAT	NP_009203.2:n.792+255_792+268delinsATTCATTCATTCAT
XM_011540550.1:c.646+255_646+268delinsATTCATTCATTCAT	XP_011538852.1:n.646+255_646+268delinsATTCATTCATTCAT
NM_007272.3:c.792+255_792+268delinsATTCATTCATTCAT MANE Select	NP_009203.2:n.792+255_792+268delinsATTCATTCATTCAT