Canonical Allele Identifier: CA353165144
Gene: TNNC1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52451416G>T , CM000665.2:g.52451416G>T GRCh38
NC_000003.11:g.52485432G>T , CM000665.1:g.52485432G>T GRCh37
NC_000003.10:g.52460472G>T NCBI36
NG_008963.1:g.7626C>A , LRG_378:g.7626C>A
NG_033112.1:g.909G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000232975.8:c.429C>A MANE Select ENSP00000232975.3:p.Asn143Lys
ENST00000232975.7:c.429C>A ENSP00000232975.3:p.Asn143Lys
ENST00000496590.1:c.297C>A ENSP00000420596.1:p.Asn99Lys
NM_003280.2:c.429C>A , LRG_378t1:c.429C>A NP_003271.1:p.Asn143Lys
NM_003280.3:c.429C>A MANE Select NP_003271.1:p.Asn143Lys