Canonical Allele Identifier: CA447974535

Gene: NKX2-5

Linked Data

• MyVariant Identifiers: chr5:g.172659578G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232575G>T , CM000667.2:g.173232575G>T	GRCh38
NC_000005.9:g.172659578G>T , CM000667.1:g.172659578G>T	GRCh37
NC_000005.8:g.172592184G>T	NCBI36
NG_013340.1:g.7738C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.969C>A MANE Select	ENSP00000327758.4:p.Ala323=
ENST00000329198.4:c.969C>A	ENSP00000327758.4:p.Ala323=
NM_001166175.1:c.*922C>A	NP_001159647.1:n.*922C>A
NM_001166176.1:c.*768C>A	NP_001159648.1:n.*768C>A
NM_004387.3:c.969C>A	NP_004378.1:p.Ala323=
NM_004387.4:c.969C>A MANE Select	NP_004378.1:p.Ala323=
NM_001166175.2:c.*922C>A	NP_001159647.1:n.*922C>A
NM_001166176.2:c.*768C>A	NP_001159648.1:n.*768C>A