Canonical Allele Identifier: CA338567674
Gene: CTRC HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375949.5:c.643G>T MANE Select ENSP00000365116.4:p.Asp215Tyr
ENST00000375943.6:c.*97G>T ENSP00000365110.2:n.*97G>T
ENST00000375949.4:c.643G>T ENSP00000365116.4:p.Asp215Tyr
ENST00000483406.1:n.407G>T
NM_007272.2:c.643G>T NP_009203.2:p.Asp215Tyr
XM_011540550.1:c.497G>T XP_011538852.1:p.Gly166Val
NM_007272.3:c.643G>T MANE Select NP_009203.2:p.Asp215Tyr