Canonical Allele Identifier: CA499670514
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145074586
MyVariant Identifiers: chr17:g.37822290G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666037G>A , CM000679.2:g.39666037G>A GRCh38
NC_000017.10:g.37822290G>A , CM000679.1:g.37822290G>A GRCh37
NC_000017.9:g.35075816G>A NCBI36
NG_008892.1:g.5692G>A , LRG_210:g.5692G>A
NG_042278.1:g.3057G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.432G>A MANE Select ENSP00000312624.2:p.Val144=
ENST00000309889.2:c.432G>A ENSP00000312624.2:p.Val144=
ENST00000578283.1:c.360G>A ENSP00000462787.1:p.Val120=
NM_003673.3:c.432G>A , LRG_210t1:c.432G>A NP_003664.1:p.Val144=
NM_003673.4:c.432G>A MANE Select NP_003664.1:p.Val144=
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