Canonical Allele Identifier: CA399304893
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665898A>T , CM000679.2:g.39665898A>T GRCh38
NC_000017.10:g.37822151A>T , CM000679.1:g.37822151A>T GRCh37
NC_000017.9:g.35075677A>T NCBI36
NG_008892.1:g.5553A>T , LRG_210:g.5553A>T
NG_042278.1:g.2918A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.293A>T MANE Select ENSP00000312624.2:p.Lys98Met
ENST00000309889.2:c.293A>T ENSP00000312624.2:p.Lys98Met
ENST00000578283.1:c.221A>T ENSP00000462787.1:p.Lys74Met
NM_003673.3:c.293A>T , LRG_210t1:c.293A>T NP_003664.1:p.Lys98Met
NM_003673.4:c.293A>T MANE Select NP_003664.1:p.Lys98Met