Canonical Allele Identifier: CA1778570272
Gene: ZMAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.40626720T>A , CM000670.2:g.40626720T>A GRCh38
NC_000008.10:g.40484239T>A , CM000670.1:g.40484239T>A GRCh37
NC_000008.9:g.40603396T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297737.11:c.578-45459A>T MANE Select ENSP00000297737.6:n.578-45459A>T
ENST00000297737.10:c.578-45459A>T ENSP00000297737.6:n.578-45459A>T
ENST00000315769.11:c.350-45459A>T ENSP00000319785.7:n.350-45459A>T
ENST00000519406.5:c.578-45459A>T ENSP00000428423.1:n.578-45459A>T
NM_001135731.1:c.350-45459A>T NP_001129203.1:n.350-45459A>T
NM_024645.2:c.578-45459A>T NP_078921.1:n.578-45459A>T
XM_011544643.1:c.608-45459A>T XP_011542945.1:n.608-45459A>T
XM_011544644.1:c.607+47984A>T XP_011542946.1:n.607+47984A>T
XM_011544645.1:c.380-45459A>T XP_011542947.1:n.380-45459A>T
XM_024447276.1:c.440-45459A>T XP_024303044.1:n.440-45459A>T
XM_024447277.1:c.440-45459A>T XP_024303045.1:n.440-45459A>T
NM_024645.3:c.578-45459A>T MANE Select NP_078921.1:n.578-45459A>T
NM_001135731.2:c.350-45459A>T NP_001129203.1:n.350-45459A>T