Canonical Allele Identifier: CA399304399
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665837C>A , CM000679.2:g.39665837C>A GRCh38
NC_000017.10:g.37822090C>A , CM000679.1:g.37822090C>A GRCh37
NC_000017.9:g.35075616C>A NCBI36
NG_008892.1:g.5492C>A , LRG_210:g.5492C>A
NG_042278.1:g.2857C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.232C>A MANE Select ENSP00000312624.2:p.Leu78Met
ENST00000309889.2:c.232C>A ENSP00000312624.2:p.Leu78Met
ENST00000578283.1:c.175-15C>A ENSP00000462787.1:n.175-15C>A
NM_003673.3:c.232C>A , LRG_210t1:c.232C>A NP_003664.1:p.Leu78Met
NM_003673.4:c.232C>A MANE Select NP_003664.1:p.Leu78Met