Canonical Allele Identifier: CA8532819

Gene: TCAP

Linked Data

• ClinVar Variation Id: 464946
• ClinVar RCV Id: RCV000524683 ; RCV002431613 ; RCV003960314
• dbSNP Id: rs756548785
• ExAC: 17:37821636 C / T
• gnomAD v2: 17-37821636-C-T
• gnomAD v3: 17-39665383-C-T
• gnomAD v4: 17-39665383-C-T
• MyVariant Identifiers: chr17:g.37821636C>T (hg19) ; chr17:g.39665383C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665383C>T , CM000679.2:g.39665383C>T	GRCh38
NC_000017.10:g.37821636C>T , CM000679.1:g.37821636C>T	GRCh37
NC_000017.9:g.35075162C>T	NCBI36
NG_008892.1:g.5038C>T , LRG_210:g.5038C>T
NG_042278.1:g.2403C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.24C>T MANE Select	ENSP00000312624.2:p.Cys8=
ENST00000309889.2:c.24C>T	ENSP00000312624.2:p.Cys8=
ENST00000578283.1:c.24C>T	ENSP00000462787.1:p.Cys8=
NM_003673.3:c.24C>T , LRG_210t1:c.24C>T	NP_003664.1:p.Cys8=
NM_003673.4:c.24C>T MANE Select	NP_003664.1:p.Cys8=