Canonical Allele Identifier: CA2643487186

Gene: CTRC

Linked Data

• gnomAD v4: 1-15445524-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445525_15445526dup , CM000663.2:g.15445525_15445526dup	GRCh38
NC_000001.10:g.15772020_15772021dup , CM000663.1:g.15772020_15772021dup	GRCh37
NC_000001.9:g.15644607_15644608dup	NCBI36
NG_009253.1:g.12083_12084dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.640-72_640-71dup MANE Select	ENSP00000365116.4:n.640-72_640-71dup
ENST00000375943.6:c.*94-72_*94-71dup	ENSP00000365110.2:n.*94-72_*94-71dup
ENST00000375949.4:c.640-72_640-71dup	ENSP00000365116.4:n.640-72_640-71dup
ENST00000483406.1:n.404-72_404-71dup
NM_007272.2:c.640-72_640-71dup	NP_009203.2:n.640-72_640-71dup
XM_011540550.1:c.494-72_494-71dup	XP_011538852.1:n.494-72_494-71dup
NM_007272.3:c.640-72_640-71dup MANE Select	NP_009203.2:n.640-72_640-71dup