Canonical Allele Identifier: CA1601617108
Gene: NKX2-5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173235035T= , CM000667.2:g.173235035T= GRCh38
NC_000005.9:g.172662038T= , CM000667.1:g.172662038T= GRCh37
NC_000005.8:g.172594644T= NCBI36
NG_013340.1:g.5278A=

Transcript Alleles

HGVS Amino-acid change
ENST00000329198.5:c.49A= MANE Select ENSP00000327758.4:p.Ile17=
ENST00000329198.4:c.49A= ENSP00000327758.4:p.Ile17=
ENST00000424406.2:c.49A= ENSP00000395378.2:p.Ile17=
ENST00000517440.1:c.49A= ENSP00000429905.1:p.Ile17=
ENST00000521848.1:c.49A= ENSP00000427906.1:p.Ile17=
NM_001166175.1:c.49A= NP_001159647.1:p.Ile17=
NM_001166176.1:c.49A= NP_001159648.1:p.Ile17=
NM_004387.3:c.49A= NP_004378.1:p.Ile17=
XM_017009071.2:c.49A= XP_016864560.1:p.Ile17=
NM_004387.4:c.49A= MANE Select NP_004378.1:p.Ile17=
NM_001166175.2:c.49A= NP_001159647.1:p.Ile17=
NM_001166176.2:c.49A= NP_001159648.1:p.Ile17=