Canonical Allele Identifier: CA2695241961

Gene: CTRC

Linked Data

• dbSNP Id: rs146762370

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446003_15446004insTC , CM000663.2:g.15446003_15446004insTC	GRCh38
NC_000001.10:g.15772498_15772499insTC , CM000663.1:g.15772498_15772499insTC	GRCh37
NC_000001.9:g.15645085_15645086insTC	NCBI36
NG_009253.1:g.12561_12562insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+254_792+255insTC MANE Select	ENSP00000365116.4:n.792+254_792+255insTC
ENST00000375943.6:c.*246+254_*246+255insTC	ENSP00000365110.2:n.*246+254_*246+255insTC
ENST00000375949.4:c.792+254_792+255insTC	ENSP00000365116.4:n.792+254_792+255insTC
ENST00000483406.1:n.556+254_556+255insTC
NM_007272.2:c.792+254_792+255insTC	NP_009203.2:n.792+254_792+255insTC
XM_011540550.1:c.646+254_646+255insTC	XP_011538852.1:n.646+254_646+255insTC
NM_007272.3:c.792+254_792+255insTC MANE Select	NP_009203.2:n.792+254_792+255insTC