Canonical Allele Identifier: CA2839377397

Gene: TNNC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52451206C>A , CM000665.2:g.52451206C>A	GRCh38
NC_000003.11:g.52485222C>A , CM000665.1:g.52485222C>A	GRCh37
NC_000003.10:g.52460262C>A	NCBI36
NG_008963.1:g.7836G>T , LRG_378:g.7836G>T
NG_033112.1:g.699C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232975.8:c.*69G>T MANE Select	ENSP00000232975.3:n.*69G>T
ENST00000232975.7:c.*69G>T	ENSP00000232975.3:n.*69G>T
NM_003280.2:c.*69G>T , LRG_378t1:c.*69G>T	NP_003271.1:n.*69G>T
NM_003280.3:c.*69G>T MANE Select	NP_003271.1:n.*69G>T