Canonical Allele Identifier: CA362160945
Gene: NKX2-5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173232654A>T , CM000667.2:g.173232654A>T GRCh38
NC_000005.9:g.172659657A>T , CM000667.1:g.172659657A>T GRCh37
NC_000005.8:g.172592263A>T NCBI36
NG_013340.1:g.7659T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.890T>A MANE Select ENSP00000327758.4:p.Val297Asp
ENST00000329198.4:c.890T>A ENSP00000327758.4:p.Val297Asp
NM_001166175.1:c.*843T>A NP_001159647.1:n.*843T>A
NM_001166176.1:c.*689T>A NP_001159648.1:n.*689T>A
NM_004387.3:c.890T>A NP_004378.1:p.Val297Asp
NM_004387.4:c.890T>A MANE Select NP_004378.1:p.Val297Asp
NM_001166175.2:c.*843T>A NP_001159647.1:n.*843T>A
NM_001166176.2:c.*689T>A NP_001159648.1:n.*689T>A