Canonical Allele Identifier: CA399302894

Gene: TCAP

Linked Data

• MyVariant Identifiers: chr17:g.37821673T>G (hg19) ; chr17:g.39665420T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665420T>G , CM000679.2:g.39665420T>G	GRCh38
NC_000017.10:g.37821673T>G , CM000679.1:g.37821673T>G	GRCh37
NC_000017.9:g.35075199T>G	NCBI36
NG_008892.1:g.5075T>G , LRG_210:g.5075T>G
NG_042278.1:g.2440T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.61T>G MANE Select	ENSP00000312624.2:p.Phe21Val
ENST00000309889.2:c.61T>G	ENSP00000312624.2:p.Phe21Val
ENST00000578283.1:c.61T>G	ENSP00000462787.1:p.Phe21Val
NM_003673.3:c.61T>G , LRG_210t1:c.61T>G	NP_003664.1:p.Phe21Val
NM_003673.4:c.61T>G MANE Select	NP_003664.1:p.Phe21Val