Canonical Allele Identifier: CA1155328673

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445691C= , CM000663.2:g.15445691C=	GRCh38
NC_000001.10:g.15772186C= , CM000663.1:g.15772186C=	GRCh37
NC_000001.9:g.15644773C=	NCBI36
NG_009253.1:g.12249C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.734C= MANE Select	ENSP00000365116.4:p.Thr245=
ENST00000375943.6:c.*188C=	ENSP00000365110.2:n.*188C=
ENST00000375949.4:c.734C=	ENSP00000365116.4:p.Thr245=
ENST00000483406.1:n.498C=
NM_007272.2:c.734C=	NP_009203.2:p.Thr245=
XM_011540550.1:c.588C=	XP_011538852.1:p.His196=
NM_007272.3:c.734C= MANE Select	NP_009203.2:p.Thr245=