Canonical Allele Identifier: CA338567741
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445630G>T , CM000663.2:g.15445630G>T GRCh38
NC_000001.10:g.15772125G>T , CM000663.1:g.15772125G>T GRCh37
NC_000001.9:g.15644712G>T NCBI36
NG_009253.1:g.12188G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.673G>T MANE Select ENSP00000365116.4:p.Glu225Ter
ENST00000375943.6:c.*127G>T ENSP00000365110.2:n.*127G>T
ENST00000375949.4:c.673G>T ENSP00000365116.4:p.Glu225Ter
ENST00000483406.1:n.437G>T
NM_007272.2:c.673G>T NP_009203.2:p.Glu225Ter
XM_011540550.1:c.527G>T XP_011538852.1:p.Gly176Val
NM_007272.3:c.673G>T MANE Select NP_009203.2:p.Glu225Ter