Canonical Allele Identifier: CA499670486
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1597805734
MyVariant Identifiers: chr17:g.37822269A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666016A>C , CM000679.2:g.39666016A>C GRCh38
NC_000017.10:g.37822269A>C , CM000679.1:g.37822269A>C GRCh37
NC_000017.9:g.35075795A>C NCBI36
NG_008892.1:g.5671A>C , LRG_210:g.5671A>C
NG_042278.1:g.3036A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.411A>C MANE Select ENSP00000312624.2:p.Thr137=
ENST00000309889.2:c.411A>C ENSP00000312624.2:p.Thr137=
ENST00000578283.1:c.339A>C ENSP00000462787.1:p.Thr113=
NM_003673.3:c.411A>C , LRG_210t1:c.411A>C NP_003664.1:p.Thr137=
NM_003673.4:c.411A>C MANE Select NP_003664.1:p.Thr137=
Search 100 bp 5'
Search 100 bp 3'