Canonical Allele Identifier: CA399306001
Gene: TCAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.37822313T>G (hg19) chr17:g.39666060T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39666060T>G , CM000679.2:g.39666060T>G GRCh38
NC_000017.10:g.37822313T>G , CM000679.1:g.37822313T>G GRCh37
NC_000017.9:g.35075839T>G NCBI36
NG_008892.1:g.5715T>G , LRG_210:g.5715T>G
NG_042278.1:g.3080T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.455T>G MANE Select ENSP00000312624.2:p.Leu152Arg
ENST00000309889.2:c.455T>G ENSP00000312624.2:p.Leu152Arg
ENST00000578283.1:c.383T>G ENSP00000462787.1:p.Leu128Arg
NM_003673.3:c.455T>G , LRG_210t1:c.455T>G NP_003664.1:p.Leu152Arg
NM_003673.4:c.455T>G MANE Select NP_003664.1:p.Leu152Arg
Search 100 bp 5'
Search 100 bp 3'