Canonical Allele Identifier: CA2259200704

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665599_39665607delinsCAAAGGGGA , CM000679.2:g.39665599_39665607delinsCAAAGGGGA	GRCh38
NC_000017.10:g.37821852_37821860delinsCAAAGGGGA , CM000679.1:g.37821852_37821860delinsCAAAGGGGA	GRCh37
NC_000017.9:g.35075378_35075386delinsCAAAGGGGA	NCBI36
NG_008892.1:g.5254_5262delinsCAAAGGGGA , LRG_210:g.5254_5262delinsCAAAGGGGA
NG_042278.1:g.2619_2627delinsCAAAGGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.111-117_111-109delinsCAAAGGGGA MANE Select	ENSP00000312624.2:n.111-117_111-109delinsCAAAGGGGA
ENST00000309889.2:c.111-117_111-109delinsCAAAGGGGA	ENSP00000312624.2:n.111-117_111-109delinsCAAAGGGGA
ENST00000578283.1:c.111-117_111-109delinsCAAAGGGGA	ENSP00000462787.1:n.111-117_111-109delinsCAAAGGGGA
NM_003673.3:c.111-117_111-109delinsCAAAGGGGA , LRG_210t1:c.111-117_111-109delinsCAAAGGGGA	NP_003664.1:n.111-117_111-109delinsCAAAGGGGA
NM_003673.4:c.111-117_111-109delinsCAAAGGGGA MANE Select	NP_003664.1:n.111-117_111-109delinsCAAAGGGGA