Canonical Allele Identifier: CA1144216841

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445962_15445963delinsTC , CM000663.2:g.15445962_15445963delinsTC	GRCh38
NC_000001.10:g.15772457_15772458delinsTC , CM000663.1:g.15772457_15772458delinsTC	GRCh37
NC_000001.9:g.15645044_15645045delinsTC	NCBI36
NG_009253.1:g.12520_12521delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+213_792+214delinsTC MANE Select	ENSP00000365116.4:n.792+213_792+214delinsTC
ENST00000375943.6:c.*246+213_*246+214delinsTC	ENSP00000365110.2:n.*246+213_*246+214delinsTC
ENST00000375949.4:c.792+213_792+214delinsTC	ENSP00000365116.4:n.792+213_792+214delinsTC
ENST00000483406.1:n.556+213_556+214delinsTC
NM_007272.2:c.792+213_792+214delinsTC	NP_009203.2:n.792+213_792+214delinsTC
XM_011540550.1:c.646+213_646+214delinsTC	XP_011538852.1:n.646+213_646+214delinsTC
NM_007272.3:c.792+213_792+214delinsTC MANE Select	NP_009203.2:n.792+213_792+214delinsTC