Canonical Allele Identifier: CA362160642

Gene: NKX2-5

Linked Data

• MyVariant Identifiers: chr5:g.172659572C>G (hg19) ; chr5:g.173232569C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232569C>G , CM000667.2:g.173232569C>G	GRCh38
NC_000005.9:g.172659572C>G , CM000667.1:g.172659572C>G	GRCh37
NC_000005.8:g.172592178C>G	NCBI36
NG_013340.1:g.7744G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.975G>C MANE Select	ENSP00000327758.4:p.Ter325Tyr
ENST00000329198.4:c.975G>C	ENSP00000327758.4:p.Ter325Tyr
NM_001166175.1:c.*928G>C	NP_001159647.1:n.*928G>C
NM_001166176.1:c.*774G>C	NP_001159648.1:n.*774G>C
NM_004387.3:c.975G>C	NP_004378.1:p.Ter325Tyr
NM_004387.4:c.975G>C MANE Select	NP_004378.1:p.Ter325Tyr
NM_001166175.2:c.*928G>C	NP_001159647.1:n.*928G>C
NM_001166176.2:c.*774G>C	NP_001159648.1:n.*774G>C