Canonical Allele Identifier: CA499889147
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs781560443
MyVariant Identifiers: chr17:g.37822122A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665869A>G , CM000679.2:g.39665869A>G GRCh38
NC_000017.10:g.37822122A>G , CM000679.1:g.37822122A>G GRCh37
NC_000017.9:g.35075648A>G NCBI36
NG_008892.1:g.5524A>G , LRG_210:g.5524A>G
NG_042278.1:g.2889A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.264A>G MANE Select ENSP00000312624.2:p.Val88=
ENST00000309889.2:c.264A>G ENSP00000312624.2:p.Val88=
ENST00000578283.1:c.192A>G ENSP00000462787.1:p.Val64=
NM_003673.3:c.264A>G , LRG_210t1:c.264A>G NP_003664.1:p.Val88=
NM_003673.4:c.264A>G MANE Select NP_003664.1:p.Val88=