Canonical Allele Identifier: CA2580070178
Community Standard Title: NM_003280.3(TNNC1):c.454+15G>A
Gene: TNNC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451376C>T , CM000665.2:g.52451376C>T GRCh38
NC_000003.11:g.52485392C>T , CM000665.1:g.52485392C>T GRCh37
NC_000003.10:g.52460432C>T NCBI36
NG_008963.1:g.7666G>A , LRG_378:g.7666G>A
NG_033112.1:g.869C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003280.3:c.454+15G>A MANE Select NP_003271.1:n.454+15G>A
ENST00000232975.8:c.454+15G>A MANE Select ENSP00000232975.3:n.454+15G>A
NM_003280.2:c.454+15G>A , LRG_378t1:c.454+15G>A NP_003271.1:n.454+15G>A
ENST00000232975.7:c.454+15G>A ENSP00000232975.3:n.454+15G>A