Canonical Allele Identifier: CA1143712593
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445958G= , CM000663.2:g.15445958G= GRCh38
NC_000001.10:g.15772453G= , CM000663.1:g.15772453G= GRCh37
NC_000001.9:g.15645040G= NCBI36
NG_009253.1:g.12516G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+209G= MANE Select ENSP00000365116.4:n.792+209G=
ENST00000375943.6:c.*246+209G= ENSP00000365110.2:n.*246+209G=
ENST00000375949.4:c.792+209G= ENSP00000365116.4:n.792+209G=
ENST00000483406.1:n.556+209G=
NM_007272.2:c.792+209G= NP_009203.2:n.792+209G=
XM_011540550.1:c.646+209G= XP_011538852.1:n.646+209G=
NM_007272.3:c.792+209G= MANE Select NP_009203.2:n.792+209G=
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