Canonical Allele Identifier: CA1155328451
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs368477746
gnomAD v4: 1-15445584-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445584C>A , CM000663.2:g.15445584C>A GRCh38
NC_000001.10:g.15772079C>A , CM000663.1:g.15772079C>A GRCh37
NC_000001.9:g.15644666C>A NCBI36
NG_009253.1:g.12142C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-13C>A MANE Select ENSP00000365116.4:n.640-13C>A
ENST00000375943.6:c.*94-13C>A ENSP00000365110.2:n.*94-13C>A
ENST00000375949.4:c.640-13C>A ENSP00000365116.4:n.640-13C>A
ENST00000483406.1:n.404-13C>A
NM_007272.2:c.640-13C>A NP_009203.2:n.640-13C>A
XM_011540550.1:c.494-13C>A XP_011538852.1:n.494-13C>A
NM_007272.3:c.640-13C>A MANE Select NP_009203.2:n.640-13C>A
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