Canonical Allele Identifier: CA1155329217

Gene: CTRC

Linked Data

• dbSNP Id: rs1708216031

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446009_15446010insGCAT , CM000663.2:g.15446009_15446010insGCAT	GRCh38
NC_000001.10:g.15772504_15772505insGCAT , CM000663.1:g.15772504_15772505insGCAT	GRCh37
NC_000001.9:g.15645091_15645092insGCAT	NCBI36
NG_009253.1:g.12567_12568insGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+260_792+261insGCAT MANE Select	ENSP00000365116.4:n.792+260_792+261insGCAT
ENST00000375943.6:c.*246+260_*246+261insGCAT	ENSP00000365110.2:n.*246+260_*246+261insGCAT
ENST00000375949.4:c.792+260_792+261insGCAT	ENSP00000365116.4:n.792+260_792+261insGCAT
ENST00000483406.1:n.556+260_556+261insGCAT
NM_007272.2:c.792+260_792+261insGCAT	NP_009203.2:n.792+260_792+261insGCAT
XM_011540550.1:c.646+260_646+261insGCAT	XP_011538852.1:n.646+260_646+261insGCAT
NM_007272.3:c.792+260_792+261insGCAT MANE Select	NP_009203.2:n.792+260_792+261insGCAT