Canonical Allele Identifier: CA1155328538

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445626G= , CM000663.2:g.15445626G=	GRCh38
NC_000001.10:g.15772121G= , CM000663.1:g.15772121G=	GRCh37
NC_000001.9:g.15644708G=	NCBI36
NG_009253.1:g.12184G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.669G= MANE Select	ENSP00000365116.4:p.Gln223=
ENST00000375943.6:c.*123G=	ENSP00000365110.2:n.*123G=
ENST00000375949.4:c.669G=	ENSP00000365116.4:p.Gln223=
ENST00000483406.1:n.433G=
NM_007272.2:c.669G=	NP_009203.2:p.Gln223=
XM_011540550.1:c.523G=	XP_011538852.1:p.Val175=
NM_007272.3:c.669G= MANE Select	NP_009203.2:p.Gln223=