Canonical Allele Identifier: CA2433183
Community Standard Title: NM_015512.5(DNAH1):c.2221A>G (p.Met741Val)
Gene: DNAH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52349002A>G , CM000665.2:g.52349002A>G GRCh38
NC_000003.11:g.52383018A>G , CM000665.1:g.52383018A>G GRCh37
NC_000003.10:g.52358058A>G NCBI36
NG_052911.1:g.37684A>G

Transcript Alleles

HGVS Amino-acid Change
NM_015512.5:c.2221A>G MANE Select NP_056327.4:p.Met741Val
ENST00000420323.7:c.2221A>G MANE Select ENSP00000401514.2:p.Met741Val
NM_015512.4:c.2221A>G NP_056327.4:p.Met741Val
ENST00000420323.6:c.2221A>G ENSP00000401514.2:p.Met741Val
ENST00000486752.5:n.2482A>G
ENST00000497875.1:n.2386A>G
XM_011533577.1:c.2221A>G XP_011531879.1:p.Met741Val
XM_017006129.1:c.2221A>G XP_016861618.1:p.Met741Val
XM_017006130.1:c.2221A>G XP_016861619.1:p.Met741Val
XM_017006131.1:c.2221A>G XP_016861620.1:p.Met741Val
XM_017006132.1:c.2221A>G XP_016861621.1:p.Met741Val
XM_017006133.1:c.2221A>G XP_016861622.1:p.Met741Val
XR_001740098.1:n.5370A>G
XR_001740099.1:n.5370A>G