Canonical Allele Identifier: CA399303585
Gene: TCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37821995A>C (hg19) chr17:g.39665742A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665742A>C , CM000679.2:g.39665742A>C GRCh38
NC_000017.10:g.37821995A>C , CM000679.1:g.37821995A>C GRCh37
NC_000017.9:g.35075521A>C NCBI36
NG_008892.1:g.5397A>C , LRG_210:g.5397A>C
NG_042278.1:g.2762A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.137A>C MANE Select ENSP00000312624.2:p.Gln46Pro
ENST00000309889.2:c.137A>C ENSP00000312624.2:p.Gln46Pro
ENST00000578283.1:c.137A>C ENSP00000462787.1:p.Gln46Pro
NM_003673.3:c.137A>C , LRG_210t1:c.137A>C NP_003664.1:p.Gln46Pro
NM_003673.4:c.137A>C MANE Select NP_003664.1:p.Gln46Pro
Search 100 bp 5'
Search 100 bp 3'