Canonical Allele Identifier: CA399305526
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1183717842
MyVariant Identifiers: chr17:g.37822253A>C (hg19) chr17:g.39666000A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666000A>C , CM000679.2:g.39666000A>C GRCh38
NC_000017.10:g.37822253A>C , CM000679.1:g.37822253A>C GRCh37
NC_000017.9:g.35075779A>C NCBI36
NG_008892.1:g.5655A>C , LRG_210:g.5655A>C
NG_042278.1:g.3020A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.395A>C MANE Select ENSP00000312624.2:p.Glu132Ala
ENST00000309889.2:c.395A>C ENSP00000312624.2:p.Glu132Ala
ENST00000578283.1:c.323A>C ENSP00000462787.1:p.Glu108Ala
NM_003673.3:c.395A>C , LRG_210t1:c.395A>C NP_003664.1:p.Glu132Ala
NM_003673.4:c.395A>C MANE Select NP_003664.1:p.Glu132Ala
Search 100 bp 5'
Search 100 bp 3'