Canonical Allele Identifier: CA2576253853

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666040_39666058del , CM000679.2:g.39666040_39666058del	GRCh38
NC_000017.10:g.37822293_37822311del , CM000679.1:g.37822293_37822311del	GRCh37
NC_000017.9:g.35075819_35075837del	NCBI36
NG_008892.1:g.5695_5713del , LRG_210:g.5695_5713del
NG_042278.1:g.3060_3078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.435_453del MANE Select	ENSP00000312624.2:p.Val146PhefsTer?
ENST00000309889.2:c.435_453del	ENSP00000312624.2:p.Val146PhefsTer?
ENST00000578283.1:c.363_381del	ENSP00000462787.1:p.Val122PhefsTer?
NM_003673.3:c.435_453del , LRG_210t1:c.435_453del	NP_003664.1:p.Val146PhefsTer?
NM_003673.4:c.435_453del MANE Select	NP_003664.1:p.Val146PhefsTer?