Canonical Allele Identifier: CA399302771
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1321392063
gnomAD v2: 17-37821643-T-C
gnomAD v4: 17-39665390-T-C
MyVariant Identifiers: chr17:g.37821643T>C (hg19) chr17:g.39665390T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665390T>C , CM000679.2:g.39665390T>C GRCh38
NC_000017.10:g.37821643T>C , CM000679.1:g.37821643T>C GRCh37
NC_000017.9:g.35075169T>C NCBI36
NG_008892.1:g.5045T>C , LRG_210:g.5045T>C
NG_042278.1:g.2410T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.31T>C MANE Select ENSP00000312624.2:p.Ser11Pro
ENST00000309889.2:c.31T>C ENSP00000312624.2:p.Ser11Pro
ENST00000578283.1:c.31T>C ENSP00000462787.1:p.Ser11Pro
NM_003673.3:c.31T>C , LRG_210t1:c.31T>C NP_003664.1:p.Ser11Pro
NM_003673.4:c.31T>C MANE Select NP_003664.1:p.Ser11Pro
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