Canonical Allele Identifier: CA1155329110

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445930_15445934delinsGTATT , CM000663.2:g.15445930_15445934delinsGTATT	GRCh38
NC_000001.10:g.15772425_15772429delinsGTATT , CM000663.1:g.15772425_15772429delinsGTATT	GRCh37
NC_000001.9:g.15645012_15645016delinsGTATT	NCBI36
NG_009253.1:g.12488_12492delinsGTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+181_792+185delinsGTATT MANE Select	ENSP00000365116.4:n.792+181_792+185delinsGTATT
ENST00000375943.6:c.*246+181_*246+185delinsGTATT	ENSP00000365110.2:n.*246+181_*246+185delinsGTATT
ENST00000375949.4:c.792+181_792+185delinsGTATT	ENSP00000365116.4:n.792+181_792+185delinsGTATT
ENST00000483406.1:n.556+181_556+185delinsGTATT
NM_007272.2:c.792+181_792+185delinsGTATT	NP_009203.2:n.792+181_792+185delinsGTATT
XM_011540550.1:c.646+181_646+185delinsGTATT	XP_011538852.1:n.646+181_646+185delinsGTATT
NM_007272.3:c.792+181_792+185delinsGTATT MANE Select	NP_009203.2:n.792+181_792+185delinsGTATT