Canonical Allele Identifier: CA3203403
Gene: DNAH5 HGNC NCBI

Linked Data

ClinVar Variation Id: 226603
dbSNP Id: rs1348690
gnomAD v2: 5-13829611-T-C
gnomAD v3: 5-13829502-T-C
gnomAD v4: 5-13829502-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13829502T>C , CM000667.2:g.13829502T>C GRCh38
NC_000005.9:g.13829611T>C , CM000667.1:g.13829611T>C GRCh37
NC_000005.8:g.13882611T>C NCBI36
NG_013081.1:g.119979A>G
NG_013081.2:g.119979A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000683090.1:n.1375+8A>G
ENST00000265104.5:c.6444+8A>G MANE Select ENSP00000265104.4:n.6444+8A>G
ENST00000681290.1:c.6399+8A>G ENSP00000505288.1:n.6399+8A>G
ENST00000265104.4:c.6444+8A>G ENSP00000265104.4:n.6444+8A>G
NM_001369.2:c.6444+8A>G NP_001360.1:n.6444+8A>G
XM_005248262.2:c.6399+8A>G XP_005248319.1:n.6399+8A>G
XM_011513990.1:c.6444+8A>G XP_011512292.1:n.6444+8A>G
XR_925598.1:n.6651+8A>G
XM_005248262.3:c.6552+8A>G XP_005248319.2:n.6552+8A>G
XM_017009177.1:c.6552+8A>G XP_016864666.1:n.6552+8A>G
XM_017009178.1:c.5457+8A>G XP_016864667.1:n.5457+8A>G
XM_017009179.2:c.5457+8A>G XP_016864668.1:n.5457+8A>G
XM_017009180.1:c.6552+8A>G XP_016864669.1:n.6552+8A>G
XM_017009181.1:c.6552+8A>G XP_016864670.1:n.6552+8A>G
XM_017009182.1:c.6552+8A>G XP_016864671.1:n.6552+8A>G
XM_017009183.1:c.6552+8A>G XP_016864672.1:n.6552+8A>G
XM_017009184.1:c.6552+8A>G XP_016864673.1:n.6552+8A>G
XM_017009185.1:c.1641+8A>G XP_016864674.1:n.1641+8A>G
XM_017009186.1:c.1194+8A>G XP_016864675.1:n.1194+8A>G
XM_017009187.1:c.6552+8A>G XP_016864676.1:n.6552+8A>G
XM_017009188.1:c.531+8A>G XP_016864677.1:n.531+8A>G
XM_024454388.1:c.5457+8A>G XP_024310156.1:n.5457+8A>G
XM_024454389.1:c.5046+8A>G XP_024310157.1:n.5046+8A>G
XR_001742034.1:n.6569+8A>G
XR_001742035.1:n.6569+8A>G
NM_001369.3:c.6444+8A>G MANE Select NP_001360.1:n.6444+8A>G