Canonical Allele Identifier: CA2809442611

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666064_39666065insG , CM000679.2:g.39666064_39666065insG	GRCh38
NC_000017.10:g.37822317_37822318insG , CM000679.1:g.37822317_37822318insG	GRCh37
NC_000017.9:g.35075843_35075844insG	NCBI36
NG_008892.1:g.5719_5720insG , LRG_210:g.5719_5720insG
NG_042278.1:g.3084_3085insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.459_460insG MANE Select	ENSP00000312624.2:p.Arg154AlafsTer?
ENST00000309889.2:c.459_460insG	ENSP00000312624.2:p.Arg154AlafsTer?
ENST00000578283.1:c.387_388insG	ENSP00000462787.1:p.Arg130AlafsTer?
NM_003673.3:c.459_460insG , LRG_210t1:c.459_460insG	NP_003664.1:p.Arg154AlafsTer?
NM_003673.4:c.459_460insG MANE Select	NP_003664.1:p.Arg154AlafsTer?