Canonical Allele Identifier: CA2840709553

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445780C>A , CM000663.2:g.15445780C>A	GRCh38
NC_000001.10:g.15772275C>A , CM000663.1:g.15772275C>A	GRCh37
NC_000001.9:g.15644862C>A	NCBI36
NG_009253.1:g.12338C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+31C>A MANE Select	ENSP00000365116.4:n.792+31C>A
ENST00000375943.6:c.*246+31C>A	ENSP00000365110.2:n.*246+31C>A
ENST00000375949.4:c.792+31C>A	ENSP00000365116.4:n.792+31C>A
ENST00000483406.1:n.556+31C>A
NM_007272.2:c.792+31C>A	NP_009203.2:n.792+31C>A
XM_011540550.1:c.646+31C>A	XP_011538852.1:n.646+31C>A
NM_007272.3:c.792+31C>A MANE Select	NP_009203.2:n.792+31C>A