Canonical Allele Identifier: CA2673266116

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13692167-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692170del , CM000667.2:g.13692170del	GRCh38
NC_000005.9:g.13692279del , CM000667.1:g.13692279del	GRCh37
NC_000005.8:g.13745279del	NCBI36
NG_013081.1:g.257313del
NG_013081.2:g.257313del

Transcript Alleles

HGVS	Amino-acid change
ENST00000683611.1:n.1057-33del
ENST00000265104.5:c.13724-33del MANE Select	ENSP00000265104.4:n.13724-33del
ENST00000681290.1:c.13679-33del	ENSP00000505288.1:n.13679-33del
ENST00000265104.4:c.13724-33del	ENSP00000265104.4:n.13724-33del
NM_001369.2:c.13724-33del	NP_001360.1:n.13724-33del
XM_005248262.2:c.13679-33del	XP_005248319.1:n.13679-33del
XM_005248262.3:c.13832-33del	XP_005248319.2:n.13832-33del
XM_017009177.1:c.13412-33del	XP_016864666.1:n.13412-33del
XM_017009178.1:c.12737-33del	XP_016864667.1:n.12737-33del
XM_017009179.2:c.12737-33del	XP_016864668.1:n.12737-33del
XM_017009185.1:c.8921-33del	XP_016864674.1:n.8921-33del
XM_017009186.1:c.8474-33del	XP_016864675.1:n.8474-33del
XM_017009188.1:c.7811-33del	XP_016864677.1:n.7811-33del
XM_024454388.1:c.12737-33del	XP_024310156.1:n.12737-33del
XM_024454389.1:c.12326-33del	XP_024310157.1:n.12326-33del
NM_001369.3:c.13724-33del MANE Select	NP_001360.1:n.13724-33del