Canonical Allele Identifier: CA1155328483
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445600G= , CM000663.2:g.15445600G= GRCh38
NC_000001.10:g.15772095G= , CM000663.1:g.15772095G= GRCh37
NC_000001.9:g.15644682G= NCBI36
NG_009253.1:g.12158G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.643G= MANE Select ENSP00000365116.4:p.Asp215=
ENST00000375943.6:c.*97G= ENSP00000365110.2:n.*97G=
ENST00000375949.4:c.643G= ENSP00000365116.4:p.Asp215=
ENST00000483406.1:n.407G=
NM_007272.2:c.643G= NP_009203.2:p.Asp215=
XM_011540550.1:c.497G= XP_011538852.1:p.Gly166=
NM_007272.3:c.643G= MANE Select NP_009203.2:p.Asp215=