Canonical Allele Identifier: CA1155329094

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445916_15445918delinsAGT , CM000663.2:g.15445916_15445918delinsAGT	GRCh38
NC_000001.10:g.15772411_15772413delinsAGT , CM000663.1:g.15772411_15772413delinsAGT	GRCh37
NC_000001.9:g.15644998_15645000delinsAGT	NCBI36
NG_009253.1:g.12474_12476delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+167_792+169delinsAGT MANE Select	ENSP00000365116.4:n.792+167_792+169delinsAGT
ENST00000375943.6:c.*246+167_*246+169delinsAGT	ENSP00000365110.2:n.*246+167_*246+169delinsAGT
ENST00000375949.4:c.792+167_792+169delinsAGT	ENSP00000365116.4:n.792+167_792+169delinsAGT
ENST00000483406.1:n.556+167_556+169delinsAGT
NM_007272.2:c.792+167_792+169delinsAGT	NP_009203.2:n.792+167_792+169delinsAGT
XM_011540550.1:c.646+167_646+169delinsAGT	XP_011538852.1:n.646+167_646+169delinsAGT
NM_007272.3:c.792+167_792+169delinsAGT MANE Select	NP_009203.2:n.792+167_792+169delinsAGT