Canonical Allele Identifier: CA889587591
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1160248307
gnomAD v3: 1-15445852-AT-A
gnomAD v4: 1-15445852-AT-A
MyVariant Identifiers: chr1:g.15772348del (hg19) chr1:g.15445853del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445855del , CM000663.2:g.15445855del GRCh38
NC_000001.10:g.15772350del , CM000663.1:g.15772350del GRCh37
NC_000001.9:g.15644937del NCBI36
NG_009253.1:g.12413del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+106del MANE Select ENSP00000365116.4:n.792+106del
ENST00000375943.6:c.*246+106del ENSP00000365110.2:n.*246+106del
ENST00000375949.4:c.792+106del ENSP00000365116.4:n.792+106del
ENST00000483406.1:n.556+106del
NM_007272.2:c.792+106del NP_009203.2:n.792+106del
XM_011540550.1:c.646+106del XP_011538852.1:n.646+106del
NM_007272.3:c.792+106del MANE Select NP_009203.2:n.792+106del
Search 100 bp 5'
Search 100 bp 3'