Canonical Allele Identifier: CA1144269619

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15446027T= , CM000663.2:g.15446027T=	GRCh38
NC_000001.10:g.15772522T= , CM000663.1:g.15772522T=	GRCh37
NC_000001.9:g.15645109T=	NCBI36
NG_009253.1:g.12585T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+278T= MANE Select	ENSP00000365116.4:n.792+278T=
ENST00000375943.6:c.*246+278T=	ENSP00000365110.2:n.*246+278T=
ENST00000375949.4:c.792+278T=	ENSP00000365116.4:n.792+278T=
ENST00000483406.1:n.556+278T=
NM_007272.2:c.792+278T=	NP_009203.2:n.792+278T=
XM_011540550.1:c.646+278T=	XP_011538852.1:n.646+278T=
NM_007272.3:c.792+278T= MANE Select	NP_009203.2:n.792+278T=