Canonical Allele Identifier: CA1155328938
Gene: CTRC HGNC NCBI

Linked Data

dbSNP Id: rs1708209648
gnomAD v4: 1-15445821-TTCAC-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.15445825_15445828del , CM000663.2:g.15445825_15445828del GRCh38
NC_000001.10:g.15772320_15772323del , CM000663.1:g.15772320_15772323del GRCh37
NC_000001.9:g.15644907_15644910del NCBI36
NG_009253.1:g.12383_12386del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375949.5:c.792+76_792+79del MANE Select ENSP00000365116.4:n.792+76_792+79del
ENST00000375943.6:c.*246+76_*246+79del ENSP00000365110.2:n.*246+76_*246+79del
ENST00000375949.4:c.792+76_792+79del ENSP00000365116.4:n.792+76_792+79del
ENST00000483406.1:n.556+76_556+79del
NM_007272.2:c.792+76_792+79del NP_009203.2:n.792+76_792+79del
XM_011540550.1:c.646+76_646+79del XP_011538852.1:n.646+76_646+79del
NM_007272.3:c.792+76_792+79del MANE Select NP_009203.2:n.792+76_792+79del
Search 100 bp 5'
Search 100 bp 3'