Canonical Allele Identifier: CA362160994
Gene: NKX2-5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232669A>C , CM000667.2:g.173232669A>C GRCh38
NC_000005.9:g.172659672A>C , CM000667.1:g.172659672A>C GRCh37
NC_000005.8:g.172592278A>C NCBI36
NG_013340.1:g.7644T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.875T>G MANE Select ENSP00000327758.4:p.Phe292Cys
ENST00000329198.4:c.875T>G ENSP00000327758.4:p.Phe292Cys
NM_001166175.1:c.*828T>G NP_001159647.1:n.*828T>G
NM_001166176.1:c.*674T>G NP_001159648.1:n.*674T>G
NM_004387.3:c.875T>G NP_004378.1:p.Phe292Cys
NM_004387.4:c.875T>G MANE Select NP_004378.1:p.Phe292Cys
NM_001166175.2:c.*828T>G NP_001159647.1:n.*828T>G
NM_001166176.2:c.*674T>G NP_001159648.1:n.*674T>G