Canonical Allele Identifier: CA74785440
Community Standard Title: NM_015512.5(DNAH1):c.10969-2A>C
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52395306A>C , CM000665.2:g.52395306A>C GRCh38
NC_000003.11:g.52429322A>C , CM000665.1:g.52429322A>C GRCh37
NC_000003.10:g.52404362A>C NCBI36
NG_052911.1:g.83988A>C

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.10969-2A>C MANE Select NP_056327.4:n.10969-2A>C
ENST00000420323.7:c.10969-2A>C MANE Select ENSP00000401514.2:n.10969-2A>C
NM_015512.4:c.10969-2A>C NP_056327.4:n.10969-2A>C
ENST00000420323.6:c.10969-2A>C ENSP00000401514.2:n.10969-2A>C
ENST00000486752.5:n.11426-2A>C
ENST00000487254.1:n.464-2A>C
ENST00000488988.5:n.2755-2A>C
ENST00000490713.5:c.1669-2A>C ENSP00000419071.1:n.1669-2A>C
XM_011533577.1:c.11038-2A>C XP_011531879.1:n.11038-2A>C
XM_017006129.1:c.11038-2A>C XP_016861618.1:n.11038-2A>C
XM_017006130.1:c.10969-2A>C XP_016861619.1:n.10969-2A>C
XM_017006131.1:c.10912-2A>C XP_016861620.1:n.10912-2A>C
XR_001740098.1:n.14187-2A>C
XR_001740099.1:n.14187-2A>C