Canonical Allele Identifier: CA338567864
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445690A>C , CM000663.2:g.15445690A>C GRCh38
NC_000001.10:g.15772185A>C , CM000663.1:g.15772185A>C GRCh37
NC_000001.9:g.15644772A>C NCBI36
NG_009253.1:g.12248A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.733A>C MANE Select ENSP00000365116.4:p.Thr245Pro
ENST00000375943.6:c.*187A>C ENSP00000365110.2:n.*187A>C
ENST00000375949.4:c.733A>C ENSP00000365116.4:p.Thr245Pro
ENST00000483406.1:n.497A>C
NM_007272.2:c.733A>C NP_009203.2:p.Thr245Pro
XM_011540550.1:c.587A>C XP_011538852.1:p.His196Pro
NM_007272.3:c.733A>C MANE Select NP_009203.2:p.Thr245Pro