Canonical Allele Identifier: CA1364863505
Gene: TNNC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451185C= , CM000665.2:g.52451185C= GRCh38
NC_000003.11:g.52485201C= , CM000665.1:g.52485201C= GRCh37
NC_000003.10:g.52460241C= NCBI36
NG_008963.1:g.7857G= , LRG_378:g.7857G=
NG_033112.1:g.678C=

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*90G= MANE Select ENSP00000232975.3:n.*90G=
ENST00000232975.7:c.*90G= ENSP00000232975.3:n.*90G=
NM_003280.2:c.*90G= , LRG_378t1:c.*90G= NP_003271.1:n.*90G=
NM_003280.3:c.*90G= MANE Select NP_003271.1:n.*90G=