Canonical Allele Identifier: CA1145650854
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440635G= , CM000663.2:g.15440635G= GRCh38
NC_000001.10:g.15767131G= , CM000663.1:g.15767131G= GRCh37
NC_000001.9:g.15639718G= NCBI36
NG_009253.1:g.7194G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.230+45G= MANE Select ENSP00000365116.4:n.230+45G=
ENST00000375943.6:c.41-1812G= ENSP00000365110.2:n.41-1812G=
ENST00000375949.4:c.230+45G= ENSP00000365116.4:n.230+45G=
ENST00000476813.5:n.53-1812G=
ENST00000483406.1:n.140+45G=
NM_007272.2:c.230+45G= NP_009203.2:n.230+45G=
XM_011540550.1:c.230+45G= XP_011538852.1:n.230+45G=
NM_007272.3:c.230+45G= MANE Select NP_009203.2:n.230+45G=
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