Canonical Allele Identifier: CA998927578
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1708213053
gnomAD v3: 1-15445929-TG-T
gnomAD v4: 1-15445929-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445930del , CM000663.2:g.15445930del GRCh38
NC_000001.10:g.15772425del , CM000663.1:g.15772425del GRCh37
NC_000001.9:g.15645012del NCBI36
NG_009253.1:g.12488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+181del MANE Select ENSP00000365116.4:n.792+181del
ENST00000375943.6:c.*246+181del ENSP00000365110.2:n.*246+181del
ENST00000375949.4:c.792+181del ENSP00000365116.4:n.792+181del
ENST00000483406.1:n.556+181del
NM_007272.2:c.792+181del NP_009203.2:n.792+181del
XM_011540550.1:c.646+181del XP_011538852.1:n.646+181del
NM_007272.3:c.792+181del MANE Select NP_009203.2:n.792+181del
Search 100 bp 5'
Search 100 bp 3'