Canonical Allele Identifier: CA1155328982
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1708210662
gnomAD v4: 1-15445845-T-TTCATTCATTTATTCAC
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445854_15445869dup , CM000663.2:g.15445854_15445869dup GRCh38
NC_000001.10:g.15772349_15772364dup , CM000663.1:g.15772349_15772364dup GRCh37
NC_000001.9:g.15644936_15644951dup NCBI36
NG_009253.1:g.12412_12427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+105_792+120dup MANE Select ENSP00000365116.4:n.792+105_792+120dup
ENST00000375943.6:c.*246+105_*246+120dup ENSP00000365110.2:n.*246+105_*246+120dup
ENST00000375949.4:c.792+105_792+120dup ENSP00000365116.4:n.792+105_792+120dup
ENST00000483406.1:n.556+105_556+120dup
NM_007272.2:c.792+105_792+120dup NP_009203.2:n.792+105_792+120dup
XM_011540550.1:c.646+105_646+120dup XP_011538852.1:n.646+105_646+120dup
NM_007272.3:c.792+105_792+120dup MANE Select NP_009203.2:n.792+105_792+120dup
Search 100 bp 5'
Search 100 bp 3'