Canonical Allele Identifier: CA1155322133
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440530_15440537delinsATACGTGT , CM000663.2:g.15440530_15440537delinsATACGTGT GRCh38
NC_000001.10:g.15767026_15767033delinsATACGTGT , CM000663.1:g.15767026_15767033delinsATACGTGT GRCh37
NC_000001.9:g.15639613_15639620delinsATACGTGT NCBI36
NG_009253.1:g.7089_7096delinsATACGTGT

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.170_177delinsATACGTGT MANE Select ENSP00000365116.4:p.His57=
ENST00000375943.6:c.41-1917_41-1910delinsATACGTGT ENSP00000365110.2:n.41-1917_41-1910delinsATACGTGT
ENST00000375949.4:c.170_177delinsATACGTGT ENSP00000365116.4:p.His57=
ENST00000476813.5:n.53-1917_53-1910delinsATACGTGT
ENST00000483406.1:n.80_87delinsATACGTGT
NM_007272.2:c.170_177delinsATACGTGT NP_009203.2:p.His57=
XM_011540550.1:c.170_177delinsATACGTGT XP_011538852.1:p.His57=
NM_007272.3:c.170_177delinsATACGTGT MANE Select NP_009203.2:p.His57=
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