Canonical Allele Identifier: CA1364863512
Gene: TNNC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451201G= , CM000665.2:g.52451201G= GRCh38
NC_000003.11:g.52485217G= , CM000665.1:g.52485217G= GRCh37
NC_000003.10:g.52460257G= NCBI36
NG_008963.1:g.7841C= , LRG_378:g.7841C=
NG_033112.1:g.694G=

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*74C= MANE Select ENSP00000232975.3:n.*74C=
ENST00000232975.7:c.*74C= ENSP00000232975.3:n.*74C=
NM_003280.2:c.*74C= , LRG_378t1:c.*74C= NP_003271.1:n.*74C=
NM_003280.3:c.*74C= MANE Select NP_003271.1:n.*74C=