Canonical Allele Identifier: CA2259200894
Gene: TCAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666064_39666076delinsTCGCTCCCTGTCC , CM000679.2:g.39666064_39666076delinsTCGCTCCCTGTCC GRCh38
NC_000017.10:g.37822317_37822329delinsTCGCTCCCTGTCC , CM000679.1:g.37822317_37822329delinsTCGCTCCCTGTCC GRCh37
NC_000017.9:g.35075843_35075855delinsTCGCTCCCTGTCC NCBI36
NG_008892.1:g.5719_5731delinsTCGCTCCCTGTCC , LRG_210:g.5719_5731delinsTCGCTCCCTGTCC
NG_042278.1:g.3084_3096delinsTCGCTCCCTGTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.459_471delinsTCGCTCCCTGTCC MANE Select ENSP00000312624.2:p.Arg153=
ENST00000309889.2:c.459_471delinsTCGCTCCCTGTCC ENSP00000312624.2:p.Arg153=
ENST00000578283.1:c.387_399delinsTCGCTCCCTGTCC ENSP00000462787.1:p.Arg129=
NM_003673.3:c.459_471delinsTCGCTCCCTGTCC , LRG_210t1:c.459_471delinsTCGCTCCCTGTCC NP_003664.1:p.Arg153=
NM_003673.4:c.459_471delinsTCGCTCCCTGTCC MANE Select NP_003664.1:p.Arg153=
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