Canonical Allele Identifier: CA1364863514
Gene: TNNC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451204C= , CM000665.2:g.52451204C= GRCh38
NC_000003.11:g.52485220C= , CM000665.1:g.52485220C= GRCh37
NC_000003.10:g.52460260C= NCBI36
NG_008963.1:g.7838G= , LRG_378:g.7838G=
NG_033112.1:g.697C=

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*71G= MANE Select ENSP00000232975.3:n.*71G=
ENST00000232975.7:c.*71G= ENSP00000232975.3:n.*71G=
NM_003280.2:c.*71G= , LRG_378t1:c.*71G= NP_003271.1:n.*71G=
NM_003280.3:c.*71G= MANE Select NP_003271.1:n.*71G=