Canonical Allele Identifier: CA2742588023
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445917_15445988del , CM000663.2:g.15445917_15445988del GRCh38
NC_000001.10:g.15772412_15772483del , CM000663.1:g.15772412_15772483del GRCh37
NC_000001.9:g.15644999_15645070del NCBI36
NG_009253.1:g.12475_12546del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+168_792+239del MANE Select ENSP00000365116.4:n.792+168_792+239del
ENST00000375943.6:c.*246+168_*246+239del ENSP00000365110.2:n.*246+168_*246+239del
ENST00000375949.4:c.792+168_792+239del ENSP00000365116.4:n.792+168_792+239del
ENST00000483406.1:n.556+168_556+239del
NM_007272.2:c.792+168_792+239del NP_009203.2:n.792+168_792+239del
XM_011540550.1:c.646+168_646+239del XP_011538852.1:n.646+168_646+239del
NM_007272.3:c.792+168_792+239del MANE Select NP_009203.2:n.792+168_792+239del