Canonical Allele Identifier: CA1155329152

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445958_15445962delinsGCATT , CM000663.2:g.15445958_15445962delinsGCATT	GRCh38
NC_000001.10:g.15772453_15772457delinsGCATT , CM000663.1:g.15772453_15772457delinsGCATT	GRCh37
NC_000001.9:g.15645040_15645044delinsGCATT	NCBI36
NG_009253.1:g.12516_12520delinsGCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+209_792+213delinsGCATT MANE Select	ENSP00000365116.4:n.792+209_792+213delinsGCATT
ENST00000375943.6:c.*246+209_*246+213delinsGCATT	ENSP00000365110.2:n.*246+209_*246+213delinsGCATT
ENST00000375949.4:c.792+209_792+213delinsGCATT	ENSP00000365116.4:n.792+209_792+213delinsGCATT
ENST00000483406.1:n.556+209_556+213delinsGCATT
NM_007272.2:c.792+209_792+213delinsGCATT	NP_009203.2:n.792+209_792+213delinsGCATT
XM_011540550.1:c.646+209_646+213delinsGCATT	XP_011538852.1:n.646+209_646+213delinsGCATT
NM_007272.3:c.792+209_792+213delinsGCATT MANE Select	NP_009203.2:n.792+209_792+213delinsGCATT