Canonical Allele Identifier: CA338565126
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15440581A>C , CM000663.2:g.15440581A>C GRCh38
NC_000001.10:g.15767077A>C , CM000663.1:g.15767077A>C GRCh37
NC_000001.9:g.15639664A>C NCBI36
NG_009253.1:g.7140A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.221A>C MANE Select ENSP00000365116.4:p.His74Pro
ENST00000375943.6:c.41-1866A>C ENSP00000365110.2:n.41-1866A>C
ENST00000375949.4:c.221A>C ENSP00000365116.4:p.His74Pro
ENST00000476813.5:n.53-1866A>C
ENST00000483406.1:n.131A>C
NM_007272.2:c.221A>C NP_009203.2:p.His74Pro
XM_011540550.1:c.221A>C XP_011538852.1:p.His74Pro
NM_007272.3:c.221A>C MANE Select NP_009203.2:p.His74Pro