Canonical Allele Identifier: CA399304869
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1390863059
gnomAD v2: 17-37822147-G-A
gnomAD v3: 17-39665894-G-A
gnomAD v4: 17-39665894-G-A
MyVariant Identifiers: chr17:g.37822147G>A (hg19) chr17:g.39665894G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665894G>A , CM000679.2:g.39665894G>A GRCh38
NC_000017.10:g.37822147G>A , CM000679.1:g.37822147G>A GRCh37
NC_000017.9:g.35075673G>A NCBI36
NG_008892.1:g.5549G>A , LRG_210:g.5549G>A
NG_042278.1:g.2914G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.289G>A MANE Select ENSP00000312624.2:p.Ala97Thr
ENST00000309889.2:c.289G>A ENSP00000312624.2:p.Ala97Thr
ENST00000578283.1:c.217G>A ENSP00000462787.1:p.Ala73Thr
NM_003673.3:c.289G>A , LRG_210t1:c.289G>A NP_003664.1:p.Ala97Thr
NM_003673.4:c.289G>A MANE Select NP_003664.1:p.Ala97Thr
Search 100 bp 5'
Search 100 bp 3'