Canonical Allele Identifier: CA1155329097

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445917_15445921delinsGTCAC , CM000663.2:g.15445917_15445921delinsGTCAC	GRCh38
NC_000001.10:g.15772412_15772416delinsGTCAC , CM000663.1:g.15772412_15772416delinsGTCAC	GRCh37
NC_000001.9:g.15644999_15645003delinsGTCAC	NCBI36
NG_009253.1:g.12475_12479delinsGTCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+168_792+172delinsGTCAC MANE Select	ENSP00000365116.4:n.792+168_792+172delinsGTCAC
ENST00000375943.6:c.*246+168_*246+172delinsGTCAC	ENSP00000365110.2:n.*246+168_*246+172delinsGTCAC
ENST00000375949.4:c.792+168_792+172delinsGTCAC	ENSP00000365116.4:n.792+168_792+172delinsGTCAC
ENST00000483406.1:n.556+168_556+172delinsGTCAC
NM_007272.2:c.792+168_792+172delinsGTCAC	NP_009203.2:n.792+168_792+172delinsGTCAC
XM_011540550.1:c.646+168_646+172delinsGTCAC	XP_011538852.1:n.646+168_646+172delinsGTCAC
NM_007272.3:c.792+168_792+172delinsGTCAC MANE Select	NP_009203.2:n.792+168_792+172delinsGTCAC