Canonical Allele Identifier: CA1155328819

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445738T= , CM000663.2:g.15445738T=	GRCh38
NC_000001.10:g.15772233T= , CM000663.1:g.15772233T=	GRCh37
NC_000001.9:g.15644820T=	NCBI36
NG_009253.1:g.12296T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.781T= MANE Select	ENSP00000365116.4:p.Trp261=
ENST00000375943.6:c.*235T=	ENSP00000365110.2:n.*235T=
ENST00000375949.4:c.781T=	ENSP00000365116.4:p.Trp261=
ENST00000483406.1:n.545T=
NM_007272.2:c.781T=	NP_009203.2:p.Trp261=
XM_011540550.1:c.635T=	XP_011538852.1:p.Leu212=
NM_007272.3:c.781T= MANE Select	NP_009203.2:p.Trp261=