Canonical Allele Identifier: CA499670332
Gene: TCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37821627G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665374G>A , CM000679.2:g.39665374G>A GRCh38
NC_000017.10:g.37821627G>A , CM000679.1:g.37821627G>A GRCh37
NC_000017.9:g.35075153G>A NCBI36
NG_008892.1:g.5029G>A , LRG_210:g.5029G>A
NG_042278.1:g.2394G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.15G>A MANE Select ENSP00000312624.2:p.Glu5=
ENST00000309889.2:c.15G>A ENSP00000312624.2:p.Glu5=
ENST00000578283.1:c.15G>A ENSP00000462787.1:p.Glu5=
NM_003673.3:c.15G>A , LRG_210t1:c.15G>A NP_003664.1:p.Glu5=
NM_003673.4:c.15G>A MANE Select NP_003664.1:p.Glu5=