Canonical Allele Identifier: CA1155329108

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445929_15445930delinsTG , CM000663.2:g.15445929_15445930delinsTG	GRCh38
NC_000001.10:g.15772424_15772425delinsTG , CM000663.1:g.15772424_15772425delinsTG	GRCh37
NC_000001.9:g.15645011_15645012delinsTG	NCBI36
NG_009253.1:g.12487_12488delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+180_792+181delinsTG MANE Select	ENSP00000365116.4:n.792+180_792+181delinsTG
ENST00000375943.6:c.*246+180_*246+181delinsTG	ENSP00000365110.2:n.*246+180_*246+181delinsTG
ENST00000375949.4:c.792+180_792+181delinsTG	ENSP00000365116.4:n.792+180_792+181delinsTG
ENST00000483406.1:n.556+180_556+181delinsTG
NM_007272.2:c.792+180_792+181delinsTG	NP_009203.2:n.792+180_792+181delinsTG
XM_011540550.1:c.646+180_646+181delinsTG	XP_011538852.1:n.646+180_646+181delinsTG
NM_007272.3:c.792+180_792+181delinsTG MANE Select	NP_009203.2:n.792+180_792+181delinsTG