Canonical Allele Identifier: CA1155328550

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445632G= , CM000663.2:g.15445632G=	GRCh38
NC_000001.10:g.15772127G= , CM000663.1:g.15772127G=	GRCh37
NC_000001.9:g.15644714G=	NCBI36
NG_009253.1:g.12190G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.675G= MANE Select	ENSP00000365116.4:p.Glu225=
ENST00000375943.6:c.*129G=	ENSP00000365110.2:n.*129G=
ENST00000375949.4:c.675G=	ENSP00000365116.4:p.Glu225=
ENST00000483406.1:n.439G=
NM_007272.2:c.675G=	NP_009203.2:p.Glu225=
XM_011540550.1:c.529G=	XP_011538852.1:p.Glu177=
NM_007272.3:c.675G= MANE Select	NP_009203.2:p.Glu225=