Canonical Allele Identifier: CA447974616

Gene: NKX2-5

Linked Data

• MyVariant Identifiers: chr5:g.172659614G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.173232611G>A , CM000667.2:g.173232611G>A	GRCh38
NC_000005.9:g.172659614G>A , CM000667.1:g.172659614G>A	GRCh37
NC_000005.8:g.172592220G>A	NCBI36
NG_013340.1:g.7702C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329198.5:c.933C>T MANE Select	ENSP00000327758.4:p.Ser311=
ENST00000329198.4:c.933C>T	ENSP00000327758.4:p.Ser311=
NM_001166175.1:c.*886C>T	NP_001159647.1:n.*886C>T
NM_001166176.1:c.*732C>T	NP_001159648.1:n.*732C>T
NM_004387.3:c.933C>T	NP_004378.1:p.Ser311=
NM_004387.4:c.933C>T MANE Select	NP_004378.1:p.Ser311=
NM_001166175.2:c.*886C>T	NP_001159647.1:n.*886C>T
NM_001166176.2:c.*732C>T	NP_001159648.1:n.*732C>T