Canonical Allele Identifier: CA889587626

Gene: CTRC

Linked Data

• dbSNP Id: rs1450600635
• MyVariant Identifiers: chr1:g.15772514_15772515insATG (hg19) ; chr1:g.15446019_15446020insATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446021_15446022insGAT , CM000663.2:g.15446021_15446022insGAT	GRCh38
NC_000001.10:g.15772516_15772517insGAT , CM000663.1:g.15772516_15772517insGAT	GRCh37
NC_000001.9:g.15645103_15645104insGAT	NCBI36
NG_009253.1:g.12579_12580insGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+272_792+273insGAT MANE Select	ENSP00000365116.4:n.792+272_792+273insGAT
ENST00000375943.6:c.*246+272_*246+273insGAT	ENSP00000365110.2:n.*246+272_*246+273insGAT
ENST00000375949.4:c.792+272_792+273insGAT	ENSP00000365116.4:n.792+272_792+273insGAT
ENST00000483406.1:n.556+272_556+273insGAT
NM_007272.2:c.792+272_792+273insGAT	NP_009203.2:n.792+272_792+273insGAT
XM_011540550.1:c.646+272_646+273insGAT	XP_011538852.1:n.646+272_646+273insGAT
NM_007272.3:c.792+272_792+273insGAT MANE Select	NP_009203.2:n.792+272_792+273insGAT