Canonical Allele Identifier: CA2259200513

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665401_39665403delinsCTG , CM000679.2:g.39665401_39665403delinsCTG	GRCh38
NC_000017.10:g.37821654_37821656delinsCTG , CM000679.1:g.37821654_37821656delinsCTG	GRCh37
NC_000017.9:g.35075180_35075182delinsCTG	NCBI36
NG_008892.1:g.5056_5058delinsCTG , LRG_210:g.5056_5058delinsCTG
NG_042278.1:g.2421_2423delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.42_44delinsCTG MANE Select	ENSP00000312624.2:p.Asn14=
ENST00000309889.2:c.42_44delinsCTG	ENSP00000312624.2:p.Asn14=
ENST00000578283.1:c.42_44delinsCTG	ENSP00000462787.1:p.Asn14=
NM_003673.3:c.42_44delinsCTG , LRG_210t1:c.42_44delinsCTG	NP_003664.1:p.Asn14=
NM_003673.4:c.42_44delinsCTG MANE Select	NP_003664.1:p.Asn14=