Canonical Allele Identifier: CA1364863518
Gene: TNNC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451214A= , CM000665.2:g.52451214A= GRCh38
NC_000003.11:g.52485230A= , CM000665.1:g.52485230A= GRCh37
NC_000003.10:g.52460270A= NCBI36
NG_008963.1:g.7828T= , LRG_378:g.7828T=
NG_033112.1:g.707A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232975.8:c.*61T= MANE Select ENSP00000232975.3:n.*61T=
ENST00000232975.7:c.*61T= ENSP00000232975.3:n.*61T=
NM_003280.2:c.*61T= , LRG_378t1:c.*61T= NP_003271.1:n.*61T=
NM_003280.3:c.*61T= MANE Select NP_003271.1:n.*61T=