Canonical Allele Identifier: CA447975245
Gene: NKX2-5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.172661937G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173234934G>A , CM000667.2:g.173234934G>A GRCh38
NC_000005.9:g.172661937G>A , CM000667.1:g.172661937G>A GRCh37
NC_000005.8:g.172594543G>A NCBI36
NG_013340.1:g.5379C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.150C>T MANE Select ENSP00000327758.4:p.Ala50=
ENST00000329198.4:c.150C>T ENSP00000327758.4:p.Ala50=
ENST00000424406.2:c.150C>T ENSP00000395378.2:p.Ala50=
ENST00000517440.1:c.150C>T ENSP00000429905.1:p.Ala50=
ENST00000521848.1:c.150C>T ENSP00000427906.1:p.Ala50=
NM_001166175.1:c.150C>T NP_001159647.1:p.Ala50=
NM_001166176.1:c.150C>T NP_001159648.1:p.Ala50=
NM_004387.3:c.150C>T NP_004378.1:p.Ala50=
XM_017009071.2:c.150C>T XP_016864560.1:p.Ala50=
NM_004387.4:c.150C>T MANE Select NP_004378.1:p.Ala50=
NM_001166175.2:c.150C>T NP_001159647.1:p.Ala50=
NM_001166176.2:c.150C>T NP_001159648.1:p.Ala50=