Canonical Allele Identifier: CA2259200846

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665978_39665993delinsGGCCAGTGTGTGGACC , CM000679.2:g.39665978_39665993delinsGGCCAGTGTGTGGACC	GRCh38
NC_000017.10:g.37822231_37822246delinsGGCCAGTGTGTGGACC , CM000679.1:g.37822231_37822246delinsGGCCAGTGTGTGGACC	GRCh37
NC_000017.9:g.35075757_35075772delinsGGCCAGTGTGTGGACC	NCBI36
NG_008892.1:g.5633_5648delinsGGCCAGTGTGTGGACC , LRG_210:g.5633_5648delinsGGCCAGTGTGTGGACC
NG_042278.1:g.2998_3013delinsGGCCAGTGTGTGGACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.373_388delinsGGCCAGTGTGTGGACC MANE Select	ENSP00000312624.2:p.Gly125=
ENST00000309889.2:c.373_388delinsGGCCAGTGTGTGGACC	ENSP00000312624.2:p.Gly125=
ENST00000578283.1:c.301_316delinsGGCCAGTGTGTGGACC	ENSP00000462787.1:p.Gly101=
NM_003673.3:c.373_388delinsGGCCAGTGTGTGGACC , LRG_210t1:c.373_388delinsGGCCAGTGTGTGGACC	NP_003664.1:p.Gly125=
NM_003673.4:c.373_388delinsGGCCAGTGTGTGGACC MANE Select	NP_003664.1:p.Gly125=