Canonical Allele Identifier: CA2739272322
Gene: CTRC HGNC NCBI

Linked Data

ClinVar Variation Id: 2864981
ClinVar RCV Id: RCV003626069

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445598_15445607del , CM000663.2:g.15445598_15445607del GRCh38
NC_000001.10:g.15772093_15772102del , CM000663.1:g.15772093_15772102del GRCh37
NC_000001.9:g.15644680_15644689del NCBI36
NG_009253.1:g.12156_12165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.641_650del
ENST00000375943.6:c.*95_*104del
ENST00000375949.4:c.641_650del
ENST00000483406.1:n.405_414del
NM_007272.2:c.641_650del
XM_011540550.1:c.495_504del
NM_007272.3:c.641_650del