Canonical Allele Identifier: CA1143479956
Gene: CTRC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440462C= , CM000663.2:g.15440462C= GRCh38
NC_000001.10:g.15766958C= , CM000663.1:g.15766958C= GRCh37
NC_000001.9:g.15639545C= NCBI36
NG_009253.1:g.7021C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.133-31C= MANE Select ENSP00000365116.4:n.133-31C=
ENST00000375943.6:c.40+1958C= ENSP00000365110.2:n.40+1958C=
ENST00000375949.4:c.133-31C= ENSP00000365116.4:n.133-31C=
ENST00000476813.5:n.52+1958C=
ENST00000483406.1:n.43-31C=
NM_007272.2:c.133-31C= NP_009203.2:n.133-31C=
XM_011540550.1:c.133-31C= XP_011538852.1:n.133-31C=
NM_007272.3:c.133-31C= MANE Select NP_009203.2:n.133-31C=
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