Canonical Allele Identifier: CA1155329042

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445890_15445894delinsGCATT , CM000663.2:g.15445890_15445894delinsGCATT	GRCh38
NC_000001.10:g.15772385_15772389delinsGCATT , CM000663.1:g.15772385_15772389delinsGCATT	GRCh37
NC_000001.9:g.15644972_15644976delinsGCATT	NCBI36
NG_009253.1:g.12448_12452delinsGCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+141_792+145delinsGCATT MANE Select	ENSP00000365116.4:n.792+141_792+145delinsGCATT
ENST00000375943.6:c.*246+141_*246+145delinsGCATT	ENSP00000365110.2:n.*246+141_*246+145delinsGCATT
ENST00000375949.4:c.792+141_792+145delinsGCATT	ENSP00000365116.4:n.792+141_792+145delinsGCATT
ENST00000483406.1:n.556+141_556+145delinsGCATT
NM_007272.2:c.792+141_792+145delinsGCATT	NP_009203.2:n.792+141_792+145delinsGCATT
XM_011540550.1:c.646+141_646+145delinsGCATT	XP_011538852.1:n.646+141_646+145delinsGCATT
NM_007272.3:c.792+141_792+145delinsGCATT MANE Select	NP_009203.2:n.792+141_792+145delinsGCATT