Canonical Allele Identifier: CA613479
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs780270629
ExAC: 1:15772274 AC / A
gnomAD v2: 1-15772274-AC-A
MyVariant Identifiers: chr1:g.15772275del (hg19) chr1:g.15445780del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445781del , CM000663.2:g.15445781del GRCh38
NC_000001.10:g.15772276del , CM000663.1:g.15772276del GRCh37
NC_000001.9:g.15644863del NCBI36
NG_009253.1:g.12339del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+32del MANE Select ENSP00000365116.4:n.792+32del
ENST00000375943.6:c.*246+32del ENSP00000365110.2:n.*246+32del
ENST00000375949.4:c.792+32del ENSP00000365116.4:n.792+32del
ENST00000483406.1:n.556+32del
NM_007272.2:c.792+32del NP_009203.2:n.792+32del
XM_011540550.1:c.646+32del XP_011538852.1:n.646+32del
NM_007272.3:c.792+32del MANE Select NP_009203.2:n.792+32del
Search 100 bp 5'
Search 100 bp 3'