Canonical Allele Identifier: CA1155328552

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445633A= , CM000663.2:g.15445633A=	GRCh38
NC_000001.10:g.15772128A= , CM000663.1:g.15772128A=	GRCh37
NC_000001.9:g.15644715A=	NCBI36
NG_009253.1:g.12191A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.676A= MANE Select	ENSP00000365116.4:p.Asn226=
ENST00000375943.6:c.*130A=	ENSP00000365110.2:n.*130A=
ENST00000375949.4:c.676A=	ENSP00000365116.4:p.Asn226=
ENST00000483406.1:n.440A=
NM_007272.2:c.676A=	NP_009203.2:p.Asn226=
XM_011540550.1:c.530A=	XP_011538852.1:p.Glu177=
NM_007272.3:c.676A= MANE Select	NP_009203.2:p.Asn226=