Canonical Allele Identifier: CA399305872
Gene: TCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37822291C>A (hg19) chr17:g.39666038C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666038C>A , CM000679.2:g.39666038C>A GRCh38
NC_000017.10:g.37822291C>A , CM000679.1:g.37822291C>A GRCh37
NC_000017.9:g.35075817C>A NCBI36
NG_008892.1:g.5693C>A , LRG_210:g.5693C>A
NG_042278.1:g.3058C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.433C>A MANE Select ENSP00000312624.2:p.Pro145Thr
ENST00000309889.2:c.433C>A ENSP00000312624.2:p.Pro145Thr
ENST00000578283.1:c.361C>A ENSP00000462787.1:p.Pro121Thr
NM_003673.3:c.433C>A , LRG_210t1:c.433C>A NP_003664.1:p.Pro145Thr
NM_003673.4:c.433C>A MANE Select NP_003664.1:p.Pro145Thr
Search 100 bp 5'
Search 100 bp 3'