Canonical Allele Identifier: CA362161711
Gene: NKX2-5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1451578
ClinVar RCV Id: RCV002007293
dbSNP Id: rs797045791
MyVariant Identifiers: chr5:g.172660035A>G (hg19) chr5:g.173233032A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173233032A>G , CM000667.2:g.173233032A>G GRCh38
NC_000005.9:g.172660035A>G , CM000667.1:g.172660035A>G GRCh37
NC_000005.8:g.172592641A>G NCBI36
NG_013340.1:g.7281T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.512T>C MANE Select ENSP00000327758.4:p.Leu171Pro
ENST00000329198.4:c.512T>C ENSP00000327758.4:p.Leu171Pro
ENST00000424406.2:c.*465T>C ENSP00000395378.2:n.*465T>C
ENST00000521848.1:c.*311T>C ENSP00000427906.1:n.*311T>C
NM_001166175.1:c.*465T>C NP_001159647.1:n.*465T>C
NM_001166176.1:c.*311T>C NP_001159648.1:n.*311T>C
NM_004387.3:c.512T>C NP_004378.1:p.Leu171Pro
NM_004387.4:c.512T>C MANE Select NP_004378.1:p.Leu171Pro
NM_001166175.2:c.*465T>C NP_001159647.1:n.*465T>C
NM_001166176.2:c.*311T>C NP_001159648.1:n.*311T>C
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