Canonical Allele Identifier: CA1147320399

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445636G= , CM000663.2:g.15445636G=	GRCh38
NC_000001.10:g.15772131G= , CM000663.1:g.15772131G=	GRCh37
NC_000001.9:g.15644718G=	NCBI36
NG_009253.1:g.12194G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.679G= MANE Select	ENSP00000365116.4:p.Gly227=
ENST00000375943.6:c.*133G=	ENSP00000365110.2:n.*133G=
ENST00000375949.4:c.679G=	ENSP00000365116.4:p.Gly227=
ENST00000483406.1:n.443G=
NM_007272.2:c.679G=	NP_009203.2:p.Gly227=
XM_011540550.1:c.533G=	XP_011538852.1:p.Arg178=
NM_007272.3:c.679G= MANE Select	NP_009203.2:p.Gly227=