Canonical Allele Identifier: CA625938771

Gene: TCAP

Linked Data

• dbSNP Id: rs1398623658
• gnomAD v2: 17-37821298-A-AGGGGAGTGGGTGGGGCAGAG
• gnomAD v3: 17-39665045-A-AGGGGAGTGGGTGGGGCAGAG
• gnomAD v4: 17-39665045-A-AGGGGAGTGGGTGGGGCAGAG
• MyVariant Identifiers: chr17:g.37821298_37821299insGGGGAGTGGGTGGGGCAGAG (hg19) ; chr17:g.39665045_39665046insGGGGAGTGGGTGGGGCAGAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665048_39665067dup , CM000679.2:g.39665048_39665067dup	GRCh38
NC_000017.10:g.37821301_37821320dup , CM000679.1:g.37821301_37821320dup	GRCh37
NC_000017.9:g.35074827_35074846dup	NCBI36
NG_008892.1:g.4703_4722dup , LRG_210:g.4703_4722dup
NG_042278.1:g.2068_2087dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-312_-293dup	ENSP00000312624.2:n.-312_-293dup