Canonical Allele Identifier: CA1155322127

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440529C= , CM000663.2:g.15440529C=	GRCh38
NC_000001.10:g.15767025C= , CM000663.1:g.15767025C=	GRCh37
NC_000001.9:g.15639612C=	NCBI36
NG_009253.1:g.7088C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.169C= MANE Select	ENSP00000365116.4:p.His57=
ENST00000375943.6:c.41-1918C=	ENSP00000365110.2:n.41-1918C=
ENST00000375949.4:c.169C=	ENSP00000365116.4:p.His57=
ENST00000476813.5:n.53-1918C=
ENST00000483406.1:n.79C=
NM_007272.2:c.169C=	NP_009203.2:p.His57=
XM_011540550.1:c.169C=	XP_011538852.1:p.His57=
NM_007272.3:c.169C= MANE Select	NP_009203.2:p.His57=