Canonical Allele Identifier: CA1155328529

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445623C= , CM000663.2:g.15445623C=	GRCh38
NC_000001.10:g.15772118C= , CM000663.1:g.15772118C=	GRCh37
NC_000001.9:g.15644705C=	NCBI36
NG_009253.1:g.12181C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.666C= MANE Select	ENSP00000365116.4:p.Cys222=
ENST00000375943.6:c.*120C=	ENSP00000365110.2:n.*120C=
ENST00000375949.4:c.666C=	ENSP00000365116.4:p.Cys222=
ENST00000483406.1:n.430C=
NM_007272.2:c.666C=	NP_009203.2:p.Cys222=
XM_011540550.1:c.520C=	XP_011538852.1:p.Pro174=
NM_007272.3:c.666C= MANE Select	NP_009203.2:p.Cys222=