Canonical Allele Identifier: CA1155328532

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445625A= , CM000663.2:g.15445625A=	GRCh38
NC_000001.10:g.15772120A= , CM000663.1:g.15772120A=	GRCh37
NC_000001.9:g.15644707A=	NCBI36
NG_009253.1:g.12183A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.668A= MANE Select	ENSP00000365116.4:p.Gln223=
ENST00000375943.6:c.*122A=	ENSP00000365110.2:n.*122A=
ENST00000375949.4:c.668A=	ENSP00000365116.4:p.Gln223=
ENST00000483406.1:n.432A=
NM_007272.2:c.668A=	NP_009203.2:p.Gln223=
XM_011540550.1:c.522A=	XP_011538852.1:p.Pro174=
NM_007272.3:c.668A= MANE Select	NP_009203.2:p.Gln223=