Canonical Allele Identifier: CA998927586

Gene: CTRC

Linked Data

• dbSNP Id: rs1708216187
• gnomAD v3: 1-15446016-A-ATTCG
• gnomAD v4: 1-15446016-A-ATTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446017_15446018insTCGT , CM000663.2:g.15446017_15446018insTCGT	GRCh38
NC_000001.10:g.15772512_15772513insTCGT , CM000663.1:g.15772512_15772513insTCGT	GRCh37
NC_000001.9:g.15645099_15645100insTCGT	NCBI36
NG_009253.1:g.12575_12576insTCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+268_792+269insTCGT MANE Select	ENSP00000365116.4:n.792+268_792+269insTCGT
ENST00000375943.6:c.*246+268_*246+269insTCGT	ENSP00000365110.2:n.*246+268_*246+269insTCGT
ENST00000375949.4:c.792+268_792+269insTCGT	ENSP00000365116.4:n.792+268_792+269insTCGT
ENST00000483406.1:n.556+268_556+269insTCGT
NM_007272.2:c.792+268_792+269insTCGT	NP_009203.2:n.792+268_792+269insTCGT
XM_011540550.1:c.646+268_646+269insTCGT	XP_011538852.1:n.646+268_646+269insTCGT
NM_007272.3:c.792+268_792+269insTCGT MANE Select	NP_009203.2:n.792+268_792+269insTCGT