Canonical Allele Identifier: CA1143414703

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445726G= , CM000663.2:g.15445726G=	GRCh38
NC_000001.10:g.15772221G= , CM000663.1:g.15772221G=	GRCh37
NC_000001.9:g.15644808G=	NCBI36
NG_009253.1:g.12284G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375949.5:c.769G= MANE Select	ENSP00000365116.4:p.Ala257=
ENST00000375943.6:c.*223G=	ENSP00000365110.2:n.*223G=
ENST00000375949.4:c.769G=	ENSP00000365116.4:p.Ala257=
ENST00000483406.1:n.533G=
NM_007272.2:c.769G=	NP_009203.2:p.Ala257=
XM_011540550.1:c.623G=	XP_011538852.1:p.Arg208=
NM_007272.3:c.769G= MANE Select	NP_009203.2:p.Ala257=