Canonical Allele Identifier: CA2733560040

Gene: TCAP

Linked Data

• dbSNP Id: rs2145074752

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666055_39666056del , CM000679.2:g.39666055_39666056del	GRCh38
NC_000017.10:g.37822308_37822309del , CM000679.1:g.37822308_37822309del	GRCh37
NC_000017.9:g.35075834_35075835del	NCBI36
NG_008892.1:g.5710_5711del , LRG_210:g.5710_5711del
NG_042278.1:g.3075_3076del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.450_451del MANE Select	ENSP00000312624.2:p.Ala151ThrfsTer?
ENST00000309889.2:c.450_451del	ENSP00000312624.2:p.Ala151ThrfsTer?
ENST00000578283.1:c.378_379del	ENSP00000462787.1:p.Ala127ThrfsTer?
NM_003673.3:c.450_451del , LRG_210t1:c.450_451del	NP_003664.1:p.Ala151ThrfsTer?
NM_003673.4:c.450_451del MANE Select	NP_003664.1:p.Ala151ThrfsTer?