Canonical Allele Identifier: CA889587490
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1025639909
gnomAD v3: 1-15445521-C-A
gnomAD v4: 1-15445521-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445521C>A , CM000663.2:g.15445521C>A GRCh38
NC_000001.10:g.15772016C>A , CM000663.1:g.15772016C>A GRCh37
NC_000001.9:g.15644603C>A NCBI36
NG_009253.1:g.12079C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-76C>A MANE Select ENSP00000365116.4:n.640-76C>A
ENST00000375943.6:c.*94-76C>A ENSP00000365110.2:n.*94-76C>A
ENST00000375949.4:c.640-76C>A ENSP00000365116.4:n.640-76C>A
ENST00000483406.1:n.404-76C>A
NM_007272.2:c.640-76C>A NP_009203.2:n.640-76C>A
XM_011540550.1:c.494-76C>A XP_011538852.1:n.494-76C>A
NM_007272.3:c.640-76C>A MANE Select NP_009203.2:n.640-76C>A