Canonical Allele Identifier: CA362163482
Gene: NKX2-5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.173234879G>T , CM000667.2:g.173234879G>T GRCh38
NC_000005.9:g.172661882G>T , CM000667.1:g.172661882G>T GRCh37
NC_000005.8:g.172594488G>T NCBI36
NG_013340.1:g.5434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000329198.5:c.205C>A MANE Select ENSP00000327758.4:p.Leu69Met
ENST00000329198.4:c.205C>A ENSP00000327758.4:p.Leu69Met
ENST00000424406.2:c.205C>A ENSP00000395378.2:p.Leu69Met
ENST00000517440.1:c.205C>A ENSP00000429905.1:p.Leu69Met
ENST00000521848.1:c.205C>A ENSP00000427906.1:p.Leu69Met
NM_001166175.1:c.205C>A NP_001159647.1:p.Leu69Met
NM_001166176.1:c.205C>A NP_001159648.1:p.Leu69Met
NM_004387.3:c.205C>A NP_004378.1:p.Leu69Met
XM_017009071.2:c.205C>A XP_016864560.1:p.Leu69Met
NM_004387.4:c.205C>A MANE Select NP_004378.1:p.Leu69Met
NM_001166175.2:c.205C>A NP_001159647.1:p.Leu69Met
NM_001166176.2:c.205C>A NP_001159648.1:p.Leu69Met