Canonical Allele Identifier: CA2578269710

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717306del , CM000667.2:g.13717306del	GRCh38
NC_000005.9:g.13717415del , CM000667.1:g.13717415del	GRCh37
NC_000005.8:g.13770415del	NCBI36
NG_013081.1:g.232175del
NG_013081.2:g.232175del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12705+9del MANE Select	ENSP00000265104.4:n.12705+9del
ENST00000681290.1:c.12660+9del	ENSP00000505288.1:n.12660+9del
ENST00000265104.4:c.12705+9del	ENSP00000265104.4:n.12705+9del
NM_001369.2:c.12705+9del	NP_001360.1:n.12705+9del
XM_005248262.2:c.12660+9del	XP_005248319.1:n.12660+9del
XM_005248262.3:c.12813+9del	XP_005248319.2:n.12813+9del
XM_017009177.1:c.12813+9del	XP_016864666.1:n.12813+9del
XM_017009178.1:c.11718+9del	XP_016864667.1:n.11718+9del
XM_017009179.2:c.11718+9del	XP_016864668.1:n.11718+9del
XM_017009180.1:c.12813+9del	XP_016864669.1:n.12813+9del
XM_017009185.1:c.7902+9del	XP_016864674.1:n.7902+9del
XM_017009186.1:c.7455+9del	XP_016864675.1:n.7455+9del
XM_017009188.1:c.6792+9del	XP_016864677.1:n.6792+9del
XM_024454388.1:c.11718+9del	XP_024310156.1:n.11718+9del
XM_024454389.1:c.11307+9del	XP_024310157.1:n.11307+9del
NM_001369.3:c.12705+9del MANE Select	NP_001360.1:n.12705+9del