Canonical Allele Identifier: CA2742588017
Gene: CTRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445797C>A , CM000663.2:g.15445797C>A GRCh38
NC_000001.10:g.15772292C>A , CM000663.1:g.15772292C>A GRCh37
NC_000001.9:g.15644879C>A NCBI36
NG_009253.1:g.12355C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+48C>A MANE Select ENSP00000365116.4:n.792+48C>A
ENST00000375943.6:c.*246+48C>A ENSP00000365110.2:n.*246+48C>A
ENST00000375949.4:c.792+48C>A ENSP00000365116.4:n.792+48C>A
ENST00000483406.1:n.556+48C>A
NM_007272.2:c.792+48C>A NP_009203.2:n.792+48C>A
XM_011540550.1:c.646+48C>A XP_011538852.1:n.646+48C>A
NM_007272.3:c.792+48C>A MANE Select NP_009203.2:n.792+48C>A