Canonical Allele Identifier: CA1143522520
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445583C= , CM000663.2:g.15445583C= GRCh38
NC_000001.10:g.15772078C= , CM000663.1:g.15772078C= GRCh37
NC_000001.9:g.15644665C= NCBI36
NG_009253.1:g.12141C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.640-14C= MANE Select ENSP00000365116.4:n.640-14C=
ENST00000375943.6:c.*94-14C= ENSP00000365110.2:n.*94-14C=
ENST00000375949.4:c.640-14C= ENSP00000365116.4:n.640-14C=
ENST00000483406.1:n.404-14C=
NM_007272.2:c.640-14C= NP_009203.2:n.640-14C=
XM_011540550.1:c.494-14C= XP_011538852.1:n.494-14C=
NM_007272.3:c.640-14C= MANE Select NP_009203.2:n.640-14C=
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