Canonical Allele Identifier: CA1155329084

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445907_15445911delinsCACTT , CM000663.2:g.15445907_15445911delinsCACTT	GRCh38
NC_000001.10:g.15772402_15772406delinsCACTT , CM000663.1:g.15772402_15772406delinsCACTT	GRCh37
NC_000001.9:g.15644989_15644993delinsCACTT	NCBI36
NG_009253.1:g.12465_12469delinsCACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+158_792+162delinsCACTT MANE Select	ENSP00000365116.4:n.792+158_792+162delinsCACTT
ENST00000375943.6:c.*246+158_*246+162delinsCACTT	ENSP00000365110.2:n.*246+158_*246+162delinsCACTT
ENST00000375949.4:c.792+158_792+162delinsCACTT	ENSP00000365116.4:n.792+158_792+162delinsCACTT
ENST00000483406.1:n.556+158_556+162delinsCACTT
NM_007272.2:c.792+158_792+162delinsCACTT	NP_009203.2:n.792+158_792+162delinsCACTT
XM_011540550.1:c.646+158_646+162delinsCACTT	XP_011538852.1:n.646+158_646+162delinsCACTT
NM_007272.3:c.792+158_792+162delinsCACTT MANE Select	NP_009203.2:n.792+158_792+162delinsCACTT