Canonical Allele Identifier: CA2673269841
Gene: DNAH5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.13769270_13769271insA , CM000667.2:g.13769270_13769271insA GRCh38
NC_000005.9:g.13769379_13769380insA , CM000667.1:g.13769379_13769380insA GRCh37
NC_000005.8:g.13822379_13822380insA NCBI36
NG_013081.1:g.180210_180211insT
NG_013081.2:g.180210_180211insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265104.5:c.9721-135_9721-134insT MANE Select ENSP00000265104.4:n.9721-135_9721-134insT
ENST00000681290.1:c.9676-135_9676-134insT ENSP00000505288.1:n.9676-135_9676-134insT
ENST00000265104.4:c.9721-135_9721-134insT ENSP00000265104.4:n.9721-135_9721-134insT
ENST00000504001.3:n.433-135_433-134insT
NM_001369.2:c.9721-135_9721-134insT NP_001360.1:n.9721-135_9721-134insT
XM_005248262.2:c.9676-135_9676-134insT XP_005248319.1:n.9676-135_9676-134insT
XM_005248262.3:c.9829-135_9829-134insT XP_005248319.2:n.9829-135_9829-134insT
XM_017009177.1:c.9829-135_9829-134insT XP_016864666.1:n.9829-135_9829-134insT
XM_017009178.1:c.8734-135_8734-134insT XP_016864667.1:n.8734-135_8734-134insT
XM_017009179.2:c.8734-135_8734-134insT XP_016864668.1:n.8734-135_8734-134insT
XM_017009180.1:c.9829-135_9829-134insT XP_016864669.1:n.9829-135_9829-134insT
XM_017009181.1:c.9829-135_9829-134insT XP_016864670.1:n.9829-135_9829-134insT
XM_017009182.1:c.9829-135_9829-134insT XP_016864671.1:n.9829-135_9829-134insT
XM_017009185.1:c.4918-135_4918-134insT XP_016864674.1:n.4918-135_4918-134insT
XM_017009186.1:c.4471-135_4471-134insT XP_016864675.1:n.4471-135_4471-134insT
XM_017009188.1:c.3808-135_3808-134insT XP_016864677.1:n.3808-135_3808-134insT
XM_024454388.1:c.8734-135_8734-134insT XP_024310156.1:n.8734-135_8734-134insT
XM_024454389.1:c.8323-135_8323-134insT XP_024310157.1:n.8323-135_8323-134insT
NM_001369.3:c.9721-135_9721-134insT MANE Select NP_001360.1:n.9721-135_9721-134insT