Canonical Allele Identifier: CA2637633062

Gene: TCAP

Linked Data

• gnomAD v4: 17-39665999-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666000del , CM000679.2:g.39666000del	GRCh38
NC_000017.10:g.37822253del , CM000679.1:g.37822253del	GRCh37
NC_000017.9:g.35075779del	NCBI36
NG_008892.1:g.5655del , LRG_210:g.5655del
NG_042278.1:g.3020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.395del MANE Select	ENSP00000312624.2:p.Glu132GlyfsTer?
ENST00000309889.2:c.395del	ENSP00000312624.2:p.Glu132GlyfsTer?
ENST00000578283.1:c.323del	ENSP00000462787.1:p.Glu108GlyfsTer?
NM_003673.3:c.395del , LRG_210t1:c.395del	NP_003664.1:p.Glu132GlyfsTer?
NM_003673.4:c.395del MANE Select	NP_003664.1:p.Glu132GlyfsTer?