Canonical Allele Identifier: CA2838889102

Gene: CTRC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15440616dup , CM000663.2:g.15440616dup	GRCh38
NC_000001.10:g.15767112dup , CM000663.1:g.15767112dup	GRCh37
NC_000001.9:g.15639699dup	NCBI36
NG_009253.1:g.7175dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.230+26dup MANE Select	ENSP00000365116.4:n.230+26dup
ENST00000375943.6:c.41-1831dup	ENSP00000365110.2:n.41-1831dup
ENST00000375949.4:c.230+26dup	ENSP00000365116.4:n.230+26dup
ENST00000476813.5:n.53-1831dup
ENST00000483406.1:n.140+26dup
NM_007272.2:c.230+26dup	NP_009203.2:n.230+26dup
XM_011540550.1:c.230+26dup	XP_011538852.1:n.230+26dup
NM_007272.3:c.230+26dup MANE Select	NP_009203.2:n.230+26dup