Canonical Allele Identifier: CA499889211
Gene: TCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37822200G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665947G>A , CM000679.2:g.39665947G>A GRCh38
NC_000017.10:g.37822200G>A , CM000679.1:g.37822200G>A GRCh37
NC_000017.9:g.35075726G>A NCBI36
NG_008892.1:g.5602G>A , LRG_210:g.5602G>A
NG_042278.1:g.2967G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.342G>A MANE Select ENSP00000312624.2:p.Gln114=
ENST00000309889.2:c.342G>A ENSP00000312624.2:p.Gln114=
ENST00000578283.1:c.270G>A ENSP00000462787.1:p.Gln90=
NM_003673.3:c.342G>A , LRG_210t1:c.342G>A NP_003664.1:p.Gln114=
NM_003673.4:c.342G>A MANE Select NP_003664.1:p.Gln114=
Search 100 bp 5'
Search 100 bp 3'