Canonical Allele Identifier: CA2673268757
Gene: DNAH5 HGNC NCBI

Linked Data

gnomAD v4: 5-13776759-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13776759C>G , CM000667.2:g.13776759C>G GRCh38
NC_000005.9:g.13776868C>G , CM000667.1:g.13776868C>G GRCh37
NC_000005.8:g.13829868C>G NCBI36
NG_013081.1:g.172722G>C
NG_013081.2:g.172722G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9106-53G>C MANE Select ENSP00000265104.4:n.9106-53G>C
ENST00000681290.1:c.9061-53G>C ENSP00000505288.1:n.9061-53G>C
ENST00000265104.4:c.9106-53G>C ENSP00000265104.4:n.9106-53G>C
NM_001369.2:c.9106-53G>C NP_001360.1:n.9106-53G>C
XM_005248262.2:c.9061-53G>C XP_005248319.1:n.9061-53G>C
XM_011513990.1:c.9101-53G>C XP_011512292.1:n.9101-53G>C
XR_925598.1:n.9177-53G>C
XM_005248262.3:c.9214-53G>C XP_005248319.2:n.9214-53G>C
XM_017009177.1:c.9214-53G>C XP_016864666.1:n.9214-53G>C
XM_017009178.1:c.8119-53G>C XP_016864667.1:n.8119-53G>C
XM_017009179.2:c.8119-53G>C XP_016864668.1:n.8119-53G>C
XM_017009180.1:c.9214-53G>C XP_016864669.1:n.9214-53G>C
XM_017009181.1:c.9214-53G>C XP_016864670.1:n.9214-53G>C
XM_017009182.1:c.9214-53G>C XP_016864671.1:n.9214-53G>C
XM_017009183.1:c.9214-53G>C XP_016864672.1:n.9214-53G>C
XM_017009184.1:c.9209-53G>C XP_016864673.1:n.9209-53G>C
XM_017009185.1:c.4303-53G>C XP_016864674.1:n.4303-53G>C
XM_017009186.1:c.3856-53G>C XP_016864675.1:n.3856-53G>C
XM_017009188.1:c.3193-53G>C XP_016864677.1:n.3193-53G>C
XM_024454388.1:c.8119-53G>C XP_024310156.1:n.8119-53G>C
XM_024454389.1:c.7708-53G>C XP_024310157.1:n.7708-53G>C
XR_001742034.1:n.9100-53G>C
XR_001742035.1:n.9095-53G>C
NM_001369.3:c.9106-53G>C MANE Select NP_001360.1:n.9106-53G>C