Canonical Allele Identifier: CA1601617109
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173235036G= , CM000667.2:g.173235036G= GRCh38
NC_000005.9:g.172662039G= , CM000667.1:g.172662039G= GRCh37
NC_000005.8:g.172594645G= NCBI36
NG_013340.1:g.5277C=

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.48C= MANE Select ENSP00000327758.4:p.Asp16=
ENST00000329198.4:c.48C= ENSP00000327758.4:p.Asp16=
ENST00000424406.2:c.48C= ENSP00000395378.2:p.Asp16=
ENST00000517440.1:c.48C= ENSP00000429905.1:p.Asp16=
ENST00000521848.1:c.48C= ENSP00000427906.1:p.Asp16=
NM_001166175.1:c.48C= NP_001159647.1:p.Asp16=
NM_001166176.1:c.48C= NP_001159648.1:p.Asp16=
NM_004387.3:c.48C= NP_004378.1:p.Asp16=
XM_017009071.2:c.48C= XP_016864560.1:p.Asp16=
NM_004387.4:c.48C= MANE Select NP_004378.1:p.Asp16=
NM_001166175.2:c.48C= NP_001159647.1:p.Asp16=
NM_001166176.2:c.48C= NP_001159648.1:p.Asp16=