Canonical Allele Identifier: CA1155329116

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445931_15445939delinsTATTTATTC , CM000663.2:g.15445931_15445939delinsTATTTATTC	GRCh38
NC_000001.10:g.15772426_15772434delinsTATTTATTC , CM000663.1:g.15772426_15772434delinsTATTTATTC	GRCh37
NC_000001.9:g.15645013_15645021delinsTATTTATTC	NCBI36
NG_009253.1:g.12489_12497delinsTATTTATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+182_792+190delinsTATTTATTC MANE Select	ENSP00000365116.4:n.792+182_792+190delinsTATTTATTC
ENST00000375943.6:c.*246+182_*246+190delinsTATTTATTC	ENSP00000365110.2:n.*246+182_*246+190delinsTATTTATTC
ENST00000375949.4:c.792+182_792+190delinsTATTTATTC	ENSP00000365116.4:n.792+182_792+190delinsTATTTATTC
ENST00000483406.1:n.556+182_556+190delinsTATTTATTC
NM_007272.2:c.792+182_792+190delinsTATTTATTC	NP_009203.2:n.792+182_792+190delinsTATTTATTC
XM_011540550.1:c.646+182_646+190delinsTATTTATTC	XP_011538852.1:n.646+182_646+190delinsTATTTATTC
NM_007272.3:c.792+182_792+190delinsTATTTATTC MANE Select	NP_009203.2:n.792+182_792+190delinsTATTTATTC