Canonical Allele Identifier: CA2673268351
Gene: DNAH5 HGNC NCBI

Linked Data

gnomAD v4: 5-13771094-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13771094A>G , CM000667.2:g.13771094A>G GRCh38
NC_000005.9:g.13771203A>G , CM000667.1:g.13771203A>G GRCh37
NC_000005.8:g.13824203A>G NCBI36
NG_013081.1:g.178387T>C
NG_013081.2:g.178387T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9374-114T>C MANE Select ENSP00000265104.4:n.9374-114T>C
ENST00000681290.1:c.9329-114T>C ENSP00000505288.1:n.9329-114T>C
ENST00000265104.4:c.9374-114T>C ENSP00000265104.4:n.9374-114T>C
ENST00000504001.3:n.85+104T>C
NM_001369.2:c.9374-114T>C NP_001360.1:n.9374-114T>C
XM_005248262.2:c.9329-114T>C XP_005248319.1:n.9329-114T>C
XM_005248262.3:c.9482-114T>C XP_005248319.2:n.9482-114T>C
XM_017009177.1:c.9482-114T>C XP_016864666.1:n.9482-114T>C
XM_017009178.1:c.8387-114T>C XP_016864667.1:n.8387-114T>C
XM_017009179.2:c.8387-114T>C XP_016864668.1:n.8387-114T>C
XM_017009180.1:c.9482-114T>C XP_016864669.1:n.9482-114T>C
XM_017009181.1:c.9482-114T>C XP_016864670.1:n.9482-114T>C
XM_017009182.1:c.9482-114T>C XP_016864671.1:n.9482-114T>C
XM_017009183.1:c.9482-114T>C XP_016864672.1:n.9482-114T>C
XM_017009185.1:c.4571-114T>C XP_016864674.1:n.4571-114T>C
XM_017009186.1:c.4124-114T>C XP_016864675.1:n.4124-114T>C
XM_017009188.1:c.3461-114T>C XP_016864677.1:n.3461-114T>C
XM_024454388.1:c.8387-114T>C XP_024310156.1:n.8387-114T>C
XM_024454389.1:c.7976-114T>C XP_024310157.1:n.7976-114T>C
NM_001369.3:c.9374-114T>C MANE Select NP_001360.1:n.9374-114T>C