Canonical Allele Identifier: CA2643487293

Gene: CTRC

Linked Data

• gnomAD v4: 1-15445808-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445809dup , CM000663.2:g.15445809dup	GRCh38
NC_000001.10:g.15772304dup , CM000663.1:g.15772304dup	GRCh37
NC_000001.9:g.15644891dup	NCBI36
NG_009253.1:g.12367dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.792+60dup MANE Select	ENSP00000365116.4:n.792+60dup
ENST00000375943.6:c.*246+60dup	ENSP00000365110.2:n.*246+60dup
ENST00000375949.4:c.792+60dup	ENSP00000365116.4:n.792+60dup
ENST00000483406.1:n.556+60dup
NM_007272.2:c.792+60dup	NP_009203.2:n.792+60dup
XM_011540550.1:c.646+60dup	XP_011538852.1:n.646+60dup
NM_007272.3:c.792+60dup MANE Select	NP_009203.2:n.792+60dup