Canonical Allele Identifier: CA521458355

Gene: CTRC

Linked Data

• dbSNP Id: rs1332346086
• gnomAD v2: 1-15772059-C-CCTGGTGGCTTATGCCCTCCCGGT
• gnomAD v3: 1-15445564-C-CCTGGTGGCTTATGCCCTCCCGGT
• gnomAD v4: 1-15445564-C-CCTGGTGGCTTATGCCCTCCCGGT
• MyVariant Identifiers: chr1:g.15772059_15772060insCTGGTGGCTTATGCCCTCCCGGT (hg19) ; chr1:g.15445564_15445565insCTGGTGGCTTATGCCCTCCCGGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15445571_15445593dup , CM000663.2:g.15445571_15445593dup	GRCh38
NC_000001.10:g.15772066_15772088dup , CM000663.1:g.15772066_15772088dup	GRCh37
NC_000001.9:g.15644653_15644675dup	NCBI36
NG_009253.1:g.12129_12151dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375949.5:c.640-26_640-4dup MANE Select	ENSP00000365116.4:n.640-26_640-4dup
ENST00000375943.6:c.*94-26_*94-4dup	ENSP00000365110.2:n.*94-26_*94-4dup
ENST00000375949.4:c.640-26_640-4dup	ENSP00000365116.4:n.640-26_640-4dup
ENST00000483406.1:n.404-26_404-4dup
NM_007272.2:c.640-26_640-4dup	NP_009203.2:n.640-26_640-4dup
XM_011540550.1:c.494-26_494-4dup	XP_011538852.1:n.494-26_494-4dup
NM_007272.3:c.640-26_640-4dup MANE Select	NP_009203.2:n.640-26_640-4dup