Canonical Allele Identifier: CA353120130
Community Standard Title: NM_015512.5(DNAH1):c.3772C>T (p.Gln1258Ter)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52356692C>T , CM000665.2:g.52356692C>T GRCh38
NC_000003.11:g.52390708C>T , CM000665.1:g.52390708C>T GRCh37
NC_000003.10:g.52365748C>T NCBI36
NG_052911.1:g.45374C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.3772C>T MANE Select NP_056327.4:p.Gln1258Ter
ENST00000420323.7:c.3772C>T MANE Select ENSP00000401514.2:p.Gln1258Ter
NM_015512.4:c.3772C>T NP_056327.4:p.Gln1258Ter
ENST00000420323.6:c.3772C>T ENSP00000401514.2:p.Gln1258Ter
ENST00000486752.5:n.4033C>T
XM_011533577.1:c.3772C>T XP_011531879.1:p.Gln1258Ter
XM_017006129.1:c.3772C>T XP_016861618.1:p.Gln1258Ter
XM_017006130.1:c.3772C>T XP_016861619.1:p.Gln1258Ter
XM_017006131.1:c.3772C>T XP_016861620.1:p.Gln1258Ter
XM_017006132.1:c.3772C>T XP_016861621.1:p.Gln1258Ter
XM_017006133.1:c.3772C>T XP_016861622.1:p.Gln1258Ter
XR_001740098.1:n.6921C>T
XR_001740099.1:n.6921C>T