Canonical Allele Identifier: CA1155328803

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445728C= , CM000663.2:g.15445728C=	GRCh38
NC_000001.10:g.15772223C= , CM000663.1:g.15772223C=	GRCh37
NC_000001.9:g.15644810C=	NCBI36
NG_009253.1:g.12286C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.771C= MANE Select	ENSP00000365116.4:p.Ala257=
ENST00000375943.6:c.*225C=	ENSP00000365110.2:n.*225C=
ENST00000375949.4:c.771C=	ENSP00000365116.4:p.Ala257=
ENST00000483406.1:n.535C=
NM_007272.2:c.771C=	NP_009203.2:p.Ala257=
XM_011540550.1:c.625C=	XP_011538852.1:p.Leu209=
NM_007272.3:c.771C= MANE Select	NP_009203.2:p.Ala257=