Canonical Allele Identifier: CA399304703
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1157780396

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665873C>G , CM000679.2:g.39665873C>G GRCh38
NC_000017.10:g.37822126C>G , CM000679.1:g.37822126C>G GRCh37
NC_000017.9:g.35075652C>G NCBI36
NG_008892.1:g.5528C>G , LRG_210:g.5528C>G
NG_042278.1:g.2893C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000309889.3:c.268C>G MANE Select ENSP00000312624.2:p.Pro90Ala
ENST00000309889.2:c.268C>G ENSP00000312624.2:p.Pro90Ala
ENST00000578283.1:c.196C>G ENSP00000462787.1:p.Pro66Ala
NM_003673.3:c.268C>G , LRG_210t1:c.268C>G NP_003664.1:p.Pro90Ala
NM_003673.4:c.268C>G MANE Select NP_003664.1:p.Pro90Ala