Canonical Allele Identifier: CA2643487364
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445909_15445916del , CM000663.2:g.15445909_15445916del GRCh38
NC_000001.10:g.15772404_15772411del , CM000663.1:g.15772404_15772411del GRCh37
NC_000001.9:g.15644991_15644998del NCBI36
NG_009253.1:g.12467_12474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+160_792+167del MANE Select ENSP00000365116.4:n.792+160_792+167del
ENST00000375943.6:c.*246+160_*246+167del ENSP00000365110.2:n.*246+160_*246+167del
ENST00000375949.4:c.792+160_792+167del ENSP00000365116.4:n.792+160_792+167del
ENST00000483406.1:n.556+160_556+167del
NM_007272.2:c.792+160_792+167del NP_009203.2:n.792+160_792+167del
XM_011540550.1:c.646+160_646+167del XP_011538852.1:n.646+160_646+167del
NM_007272.3:c.792+160_792+167del MANE Select NP_009203.2:n.792+160_792+167del