Canonical Allele Identifier: CA1073400452
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13886154_13886155insAAAAAAAAAAAAACAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000667.2:g.13886154_13886155insAAAAAAAAAAAAACAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000005.9:g.13886263_13886264insAAAAAAAAAAAAACAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000667.1:g.13886263_13886264insAAAAAAAAAAAAACAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000005.8:g.13939263_13939264insAAAAAAAAAAAAACAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_013081.1:g.63345_63346insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_013081.2:g.63345_63346insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000265104.4:n.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTG...
ENST00000681290.1:c.2533-7_2533-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000505288.1:n.2533-7_2533-6insTTTTTTTTTTTTTTTTTTATTTTTG...
ENST00000265104.4:c.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000265104.4:n.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTG...
NM_001369.2:c.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_001360.1:n.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTT...
XM_005248262.2:c.2533-7_2533-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005248319.1:n.2533-7_2533-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_011513990.1:c.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011512292.1:n.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XR_925598.1:n.2785-7_2785-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005248262.3:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005248319.2:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009177.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864666.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009178.1:c.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864667.1:n.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009179.2:c.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864668.1:n.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009180.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864669.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009181.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864670.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009182.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864671.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009183.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864672.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009184.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864673.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_017009187.1:c.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016864676.1:n.2686-7_2686-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_024454388.1:c.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_024310156.1:n.1591-7_1591-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XM_024454389.1:c.1180-7_1180-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_024310157.1:n.1180-7_1180-6insTTTTTTTTTTTTTTTTTTATTTTTGTTT...
XR_001742034.1:n.2703-7_2703-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_001742035.1:n.2703-7_2703-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001369.3:c.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_001360.1:n.2578-7_2578-6insTTTTTTTTTTTTTTTTTTATTTTTGTTTTTT...