Canonical Allele Identifier: CA353123207
Community Standard Title: NM_015512.5(DNAH1):c.3980+1G>C
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52357736G>C , CM000665.2:g.52357736G>C GRCh38
NC_000003.11:g.52391752G>C , CM000665.1:g.52391752G>C GRCh37
NC_000003.10:g.52366792G>C NCBI36
NG_052911.1:g.46418G>C

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.3980+1G>C MANE Select NP_056327.4:n.3980+1G>C
ENST00000420323.7:c.3980+1G>C MANE Select ENSP00000401514.2:n.3980+1G>C
NM_015512.4:c.3980+1G>C NP_056327.4:n.3980+1G>C
ENST00000420323.6:c.3980+1G>C ENSP00000401514.2:n.3980+1G>C
ENST00000486752.5:n.4241+1G>C
XM_011533577.1:c.3980+1G>C XP_011531879.1:n.3980+1G>C
XM_017006129.1:c.3980+1G>C XP_016861618.1:n.3980+1G>C
XM_017006130.1:c.3980+1G>C XP_016861619.1:n.3980+1G>C
XM_017006131.1:c.3980+1G>C XP_016861620.1:n.3980+1G>C
XM_017006132.1:c.3980+1G>C XP_016861621.1:n.3980+1G>C
XM_017006133.1:c.3980+1G>C XP_016861622.1:n.3980+1G>C
XR_001740098.1:n.7129+1G>C
XR_001740099.1:n.7129+1G>C