Canonical Allele Identifier: CA2765348412

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769266_13769272del , CM000667.2:g.13769266_13769272del	GRCh38
NC_000005.9:g.13769375_13769381del , CM000667.1:g.13769375_13769381del	GRCh37
NC_000005.8:g.13822375_13822381del	NCBI36
NG_013081.1:g.180209_180215del
NG_013081.2:g.180209_180215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9721-136_9721-130del MANE Select	ENSP00000265104.4:n.9721-136_9721-130del
ENST00000681290.1:c.9676-136_9676-130del	ENSP00000505288.1:n.9676-136_9676-130del
ENST00000265104.4:c.9721-136_9721-130del	ENSP00000265104.4:n.9721-136_9721-130del
ENST00000504001.3:n.433-136_433-130del
NM_001369.2:c.9721-136_9721-130del	NP_001360.1:n.9721-136_9721-130del
XM_005248262.2:c.9676-136_9676-130del	XP_005248319.1:n.9676-136_9676-130del
XM_005248262.3:c.9829-136_9829-130del	XP_005248319.2:n.9829-136_9829-130del
XM_017009177.1:c.9829-136_9829-130del	XP_016864666.1:n.9829-136_9829-130del
XM_017009178.1:c.8734-136_8734-130del	XP_016864667.1:n.8734-136_8734-130del
XM_017009179.2:c.8734-136_8734-130del	XP_016864668.1:n.8734-136_8734-130del
XM_017009180.1:c.9829-136_9829-130del	XP_016864669.1:n.9829-136_9829-130del
XM_017009181.1:c.9829-136_9829-130del	XP_016864670.1:n.9829-136_9829-130del
XM_017009182.1:c.9829-136_9829-130del	XP_016864671.1:n.9829-136_9829-130del
XM_017009185.1:c.4918-136_4918-130del	XP_016864674.1:n.4918-136_4918-130del
XM_017009186.1:c.4471-136_4471-130del	XP_016864675.1:n.4471-136_4471-130del
XM_017009188.1:c.3808-136_3808-130del	XP_016864677.1:n.3808-136_3808-130del
XM_024454388.1:c.8734-136_8734-130del	XP_024310156.1:n.8734-136_8734-130del
XM_024454389.1:c.8323-136_8323-130del	XP_024310157.1:n.8323-136_8323-130del
NM_001369.3:c.9721-136_9721-130del MANE Select	NP_001360.1:n.9721-136_9721-130del