Canonical Allele Identifier: CA2643487283
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445805_15445820del , CM000663.2:g.15445805_15445820del GRCh38
NC_000001.10:g.15772300_15772315del , CM000663.1:g.15772300_15772315del GRCh37
NC_000001.9:g.15644887_15644902del NCBI36
NG_009253.1:g.12363_12378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+56_792+71del MANE Select ENSP00000365116.4:n.792+56_792+71del
ENST00000375943.6:c.*246+56_*246+71del ENSP00000365110.2:n.*246+56_*246+71del
ENST00000375949.4:c.792+56_792+71del ENSP00000365116.4:n.792+56_792+71del
ENST00000483406.1:n.556+56_556+71del
NM_007272.2:c.792+56_792+71del NP_009203.2:n.792+56_792+71del
XM_011540550.1:c.646+56_646+71del XP_011538852.1:n.646+56_646+71del
NM_007272.3:c.792+56_792+71del MANE Select NP_009203.2:n.792+56_792+71del