Canonical Allele Identifier: CA399305569

Gene: TCAP

Linked Data

• gnomAD v4: 17-39666008-G-T
• MyVariant Identifiers: chr17:g.37822261G>T (hg19) ; chr17:g.39666008G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666008G>T , CM000679.2:g.39666008G>T	GRCh38
NC_000017.10:g.37822261G>T , CM000679.1:g.37822261G>T	GRCh37
NC_000017.9:g.35075787G>T	NCBI36
NG_008892.1:g.5663G>T , LRG_210:g.5663G>T
NG_042278.1:g.3028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.403G>T MANE Select	ENSP00000312624.2:p.Glu135Ter
ENST00000309889.2:c.403G>T	ENSP00000312624.2:p.Glu135Ter
ENST00000578283.1:c.331G>T	ENSP00000462787.1:p.Glu111Ter
NM_003673.3:c.403G>T , LRG_210t1:c.403G>T	NP_003664.1:p.Glu135Ter
NM_003673.4:c.403G>T MANE Select	NP_003664.1:p.Glu135Ter