Canonical Allele Identifier: CA1155328608

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445656C= , CM000663.2:g.15445656C=	GRCh38
NC_000001.10:g.15772151C= , CM000663.1:g.15772151C=	GRCh37
NC_000001.9:g.15644738C=	NCBI36
NG_009253.1:g.12214C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.699C= MANE Select	ENSP00000365116.4:p.Gly233=
ENST00000375943.6:c.*153C=	ENSP00000365110.2:n.*153C=
ENST00000375949.4:c.699C=	ENSP00000365116.4:p.Gly233=
ENST00000483406.1:n.463C=
NM_007272.2:c.699C=	NP_009203.2:p.Gly233=
XM_011540550.1:c.553C=	XP_011538852.1:p.His185=
NM_007272.3:c.699C= MANE Select	NP_009203.2:p.Gly233=