Canonical Allele Identifier: CA1155328618

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445661T= , CM000663.2:g.15445661T=	GRCh38
NC_000001.10:g.15772156T= , CM000663.1:g.15772156T=	GRCh37
NC_000001.9:g.15644743T=	NCBI36
NG_009253.1:g.12219T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.704T= MANE Select	ENSP00000365116.4:p.Val235=
ENST00000375943.6:c.*158T=	ENSP00000365110.2:n.*158T=
ENST00000375949.4:c.704T=	ENSP00000365116.4:p.Val235=
ENST00000483406.1:n.468T=
NM_007272.2:c.704T=	NP_009203.2:p.Val235=
XM_011540550.1:c.558T=	XP_011538852.1:p.Arg186=
NM_007272.3:c.704T= MANE Select	NP_009203.2:p.Val235=