Canonical Allele Identifier: CA399305927
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666048A>C , CM000679.2:g.39666048A>C GRCh38
NC_000017.10:g.37822301A>C , CM000679.1:g.37822301A>C GRCh37
NC_000017.9:g.35075827A>C NCBI36
NG_008892.1:g.5703A>C , LRG_210:g.5703A>C
NG_042278.1:g.3068A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.443A>C MANE Select ENSP00000312624.2:p.Lys148Thr
ENST00000309889.2:c.443A>C ENSP00000312624.2:p.Lys148Thr
ENST00000578283.1:c.371A>C ENSP00000462787.1:p.Lys124Thr
NM_003673.3:c.443A>C , LRG_210t1:c.443A>C NP_003664.1:p.Lys148Thr
NM_003673.4:c.443A>C MANE Select NP_003664.1:p.Lys148Thr