Canonical Allele Identifier: CA1155328792

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445725C= , CM000663.2:g.15445725C=	GRCh38
NC_000001.10:g.15772220C= , CM000663.1:g.15772220C=	GRCh37
NC_000001.9:g.15644807C=	NCBI36
NG_009253.1:g.12283C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.768C= MANE Select	ENSP00000365116.4:p.Ser256=
ENST00000375943.6:c.*222C=	ENSP00000365110.2:n.*222C=
ENST00000375949.4:c.768C=	ENSP00000365116.4:p.Ser256=
ENST00000483406.1:n.532C=
NM_007272.2:c.768C=	NP_009203.2:p.Ser256=
XM_011540550.1:c.622C=	XP_011538852.1:p.Arg208=
NM_007272.3:c.768C= MANE Select	NP_009203.2:p.Ser256=