Canonical Allele Identifier: CA916116174

Gene: CTRC

Linked Data

• dbSNP Id: rs1553135010

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446011_15446012insCATT , CM000663.2:g.15446011_15446012insCATT	GRCh38
NC_000001.10:g.15772506_15772507insCATT , CM000663.1:g.15772506_15772507insCATT	GRCh37
NC_000001.9:g.15645093_15645094insCATT	NCBI36
NG_009253.1:g.12569_12570insCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+262_792+263insCATT MANE Select	ENSP00000365116.4:n.792+262_792+263insCATT
ENST00000375943.6:c.*246+262_*246+263insCATT	ENSP00000365110.2:n.*246+262_*246+263insCATT
ENST00000375949.4:c.792+262_792+263insCATT	ENSP00000365116.4:n.792+262_792+263insCATT
ENST00000483406.1:n.556+262_556+263insCATT
NM_007272.2:c.792+262_792+263insCATT	NP_009203.2:n.792+262_792+263insCATT
XM_011540550.1:c.646+262_646+263insCATT	XP_011538852.1:n.646+262_646+263insCATT
NM_007272.3:c.792+262_792+263insCATT MANE Select	NP_009203.2:n.792+262_792+263insCATT