Canonical Allele Identifier: CA1155322167

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440541G= , CM000663.2:g.15440541G=	GRCh38
NC_000001.10:g.15767037G= , CM000663.1:g.15767037G=	GRCh37
NC_000001.9:g.15639624G=	NCBI36
NG_009253.1:g.7100G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.181G= MANE Select	ENSP00000365116.4:p.Gly61=
ENST00000375943.6:c.41-1906G=	ENSP00000365110.2:n.41-1906G=
ENST00000375949.4:c.181G=	ENSP00000365116.4:p.Gly61=
ENST00000476813.5:n.53-1906G=
ENST00000483406.1:n.91G=
NM_007272.2:c.181G=	NP_009203.2:p.Gly61=
XM_011540550.1:c.181G=	XP_011538852.1:p.Gly61=
NM_007272.3:c.181G= MANE Select	NP_009203.2:p.Gly61=