Canonical Allele Identifier: CA399305006

Gene: TCAP

Linked Data

• dbSNP Id: rs1597805597
• MyVariant Identifiers: chr17:g.37822162A>G (hg19) ; chr17:g.39665909A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665909A>G , CM000679.2:g.39665909A>G	GRCh38
NC_000017.10:g.37822162A>G , CM000679.1:g.37822162A>G	GRCh37
NC_000017.9:g.35075688A>G	NCBI36
NG_008892.1:g.5564A>G , LRG_210:g.5564A>G
NG_042278.1:g.2929A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.304A>G MANE Select	ENSP00000312624.2:p.Thr102Ala
ENST00000309889.2:c.304A>G	ENSP00000312624.2:p.Thr102Ala
ENST00000578283.1:c.232A>G	ENSP00000462787.1:p.Thr78Ala
NM_003673.3:c.304A>G , LRG_210t1:c.304A>G	NP_003664.1:p.Thr102Ala
NM_003673.4:c.304A>G MANE Select	NP_003664.1:p.Thr102Ala