Canonical Allele Identifier: CA1155322171

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440543G= , CM000663.2:g.15440543G=	GRCh38
NC_000001.10:g.15767039G= , CM000663.1:g.15767039G=	GRCh37
NC_000001.9:g.15639626G=	NCBI36
NG_009253.1:g.7102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.183G= MANE Select	ENSP00000365116.4:p.Gly61=
ENST00000375943.6:c.41-1904G=	ENSP00000365110.2:n.41-1904G=
ENST00000375949.4:c.183G=	ENSP00000365116.4:p.Gly61=
ENST00000476813.5:n.53-1904G=
ENST00000483406.1:n.93G=
NM_007272.2:c.183G=	NP_009203.2:p.Gly61=
XM_011540550.1:c.183G=	XP_011538852.1:p.Gly61=
NM_007272.3:c.183G= MANE Select	NP_009203.2:p.Gly61=