Canonical Allele Identifier: CA889549313
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1228156388
MyVariant Identifiers: chr1:g.15767027_15767033del (hg19) chr1:g.15440531_15440537del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440531_15440537del , CM000663.2:g.15440531_15440537del GRCh38
NC_000001.10:g.15767027_15767033del , CM000663.1:g.15767027_15767033del GRCh37
NC_000001.9:g.15639614_15639620del NCBI36
NG_009253.1:g.7090_7096del

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.171_177del MANE Select ENSP00000365116.4:p.His57GlnfsTer5
ENST00000375943.6:c.41-1916_41-1910del ENSP00000365110.2:n.41-1916_41-1910del
ENST00000375949.4:c.171_177del ENSP00000365116.4:p.His57GlnfsTer5
ENST00000476813.5:n.53-1916_53-1910del
ENST00000483406.1:n.81_87del
NM_007272.2:c.171_177del NP_009203.2:p.His57GlnfsTer5
XM_011540550.1:c.171_177del XP_011538852.1:p.His57GlnfsTer5
NM_007272.3:c.171_177del MANE Select NP_009203.2:p.His57GlnfsTer5
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