Canonical Allele Identifier: CA2259200841

Gene: TCAP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665965_39665966delinsGA , CM000679.2:g.39665965_39665966delinsGA	GRCh38
NC_000017.10:g.37822218_37822219delinsGA , CM000679.1:g.37822218_37822219delinsGA	GRCh37
NC_000017.9:g.35075744_35075745delinsGA	NCBI36
NG_008892.1:g.5620_5621delinsGA , LRG_210:g.5620_5621delinsGA
NG_042278.1:g.2985_2986delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.360_361delinsGA MANE Select	ENSP00000312624.2:p.Glu120=
ENST00000309889.2:c.360_361delinsGA	ENSP00000312624.2:p.Glu120=
ENST00000578283.1:c.288_289delinsGA	ENSP00000462787.1:p.Glu96=
NM_003673.3:c.360_361delinsGA , LRG_210t1:c.360_361delinsGA	NP_003664.1:p.Glu120=
NM_003673.4:c.360_361delinsGA MANE Select	NP_003664.1:p.Glu120=