Canonical Allele Identifier: CA2643485550
Gene: CTRC HGNC NCBI

Linked Data

gnomAD v4: 1-15440609-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440609C>A , CM000663.2:g.15440609C>A GRCh38
NC_000001.10:g.15767105C>A , CM000663.1:g.15767105C>A GRCh37
NC_000001.9:g.15639692C>A NCBI36
NG_009253.1:g.7168C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.230+19C>A MANE Select ENSP00000365116.4:n.230+19C>A
ENST00000375943.6:c.41-1838C>A ENSP00000365110.2:n.41-1838C>A
ENST00000375949.4:c.230+19C>A ENSP00000365116.4:n.230+19C>A
ENST00000476813.5:n.53-1838C>A
ENST00000483406.1:n.140+19C>A
NM_007272.2:c.230+19C>A NP_009203.2:n.230+19C>A
XM_011540550.1:c.230+19C>A XP_011538852.1:n.230+19C>A
NM_007272.3:c.230+19C>A MANE Select NP_009203.2:n.230+19C>A
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