Canonical Allele Identifier: CA399304116
Gene: TCAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665805T>G , CM000679.2:g.39665805T>G GRCh38
NC_000017.10:g.37822058T>G , CM000679.1:g.37822058T>G GRCh37
NC_000017.9:g.35075584T>G NCBI36
NG_008892.1:g.5460T>G , LRG_210:g.5460T>G
NG_042278.1:g.2825T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.200T>G MANE Select ENSP00000312624.2:p.Leu67Arg
ENST00000309889.2:c.200T>G ENSP00000312624.2:p.Leu67Arg
ENST00000578283.1:c.174+26T>G ENSP00000462787.1:n.174+26T>G
NM_003673.3:c.200T>G , LRG_210t1:c.200T>G NP_003664.1:p.Leu67Arg
NM_003673.4:c.200T>G MANE Select NP_003664.1:p.Leu67Arg