Canonical Allele Identifier: CA399302737
Gene: TCAP HGNC NCBI

Linked Data

gnomAD v4: 17-39665379-G-A
MyVariant Identifiers: chr17:g.37821632G>A (hg19) chr17:g.39665379G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665379G>A , CM000679.2:g.39665379G>A GRCh38
NC_000017.10:g.37821632G>A , CM000679.1:g.37821632G>A GRCh37
NC_000017.9:g.35075158G>A NCBI36
NG_008892.1:g.5034G>A , LRG_210:g.5034G>A
NG_042278.1:g.2399G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.20G>A MANE Select ENSP00000312624.2:p.Ser7Asn
ENST00000309889.2:c.20G>A ENSP00000312624.2:p.Ser7Asn
ENST00000578283.1:c.20G>A ENSP00000462787.1:p.Ser7Asn
NM_003673.3:c.20G>A , LRG_210t1:c.20G>A NP_003664.1:p.Ser7Asn
NM_003673.4:c.20G>A MANE Select NP_003664.1:p.Ser7Asn
Search 100 bp 5'
Search 100 bp 3'