Canonical Allele Identifier: CA1155328787

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445724C= , CM000663.2:g.15445724C=	GRCh38
NC_000001.10:g.15772219C= , CM000663.1:g.15772219C=	GRCh37
NC_000001.9:g.15644806C=	NCBI36
NG_009253.1:g.12282C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.767C= MANE Select	ENSP00000365116.4:p.Ser256=
ENST00000375943.6:c.*221C=	ENSP00000365110.2:n.*221C=
ENST00000375949.4:c.767C=	ENSP00000365116.4:p.Ser256=
ENST00000483406.1:n.531C=
NM_007272.2:c.767C=	NP_009203.2:p.Ser256=
XM_011540550.1:c.621C=	XP_011538852.1:p.Val207=
NM_007272.3:c.767C= MANE Select	NP_009203.2:p.Ser256=