Canonical Allele Identifier: CA362161713
Gene: NKX2-5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.172660036G>C (hg19) chr5:g.173233033G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173233033G>C , CM000667.2:g.173233033G>C GRCh38
NC_000005.9:g.172660036G>C , CM000667.1:g.172660036G>C GRCh37
NC_000005.8:g.172592642G>C NCBI36
NG_013340.1:g.7280C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.511C>G MANE Select ENSP00000327758.4:p.Leu171Val
ENST00000329198.4:c.511C>G ENSP00000327758.4:p.Leu171Val
ENST00000424406.2:c.*464C>G ENSP00000395378.2:n.*464C>G
ENST00000521848.1:c.*310C>G ENSP00000427906.1:n.*310C>G
NM_001166175.1:c.*464C>G NP_001159647.1:n.*464C>G
NM_001166176.1:c.*310C>G NP_001159648.1:n.*310C>G
NM_004387.3:c.511C>G NP_004378.1:p.Leu171Val
NM_004387.4:c.511C>G MANE Select NP_004378.1:p.Leu171Val
NM_001166175.2:c.*464C>G NP_001159647.1:n.*464C>G
NM_001166176.2:c.*310C>G NP_001159648.1:n.*310C>G
Search 100 bp 5'
Search 100 bp 3'