Canonical Allele Identifier: CA1084495546
Gene: NKX2-5 HGNC NCBI

Linked Data

dbSNP Id: rs1561618893

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232558G>C , CM000667.2:g.173232558G>C GRCh38
NC_000005.9:g.172659561G>C , CM000667.1:g.172659561G>C GRCh37
NC_000005.8:g.172592167G>C NCBI36
NG_013340.1:g.7755C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.*11C>G MANE Select ENSP00000327758.4:n.*11C>G
ENST00000329198.4:c.*11C>G ENSP00000327758.4:n.*11C>G
NM_001166175.1:c.*939C>G NP_001159647.1:n.*939C>G
NM_001166176.1:c.*785C>G NP_001159648.1:n.*785C>G
NM_004387.3:c.*11C>G NP_004378.1:n.*11C>G
NM_004387.4:c.*11C>G MANE Select NP_004378.1:n.*11C>G
NM_001166175.2:c.*939C>G NP_001159647.1:n.*939C>G
NM_001166176.2:c.*785C>G NP_001159648.1:n.*785C>G