Canonical Allele Identifier: CA1528423564

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753559_13753563delinsAAAAC , CM000667.2:g.13753559_13753563delinsAAAAC	GRCh38
NC_000005.9:g.13753668_13753672delinsAAAAC , CM000667.1:g.13753668_13753672delinsAAAAC	GRCh37
NC_000005.8:g.13806668_13806672delinsAAAAC	NCBI36
NG_013081.1:g.195918_195922delinsGTTTT
NG_013081.2:g.195918_195922delinsGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10556-14_10556-10delinsGTTTT MANE Select	ENSP00000265104.4:n.10556-14_10556-10delinsGTTTT
ENST00000681290.1:c.10511-14_10511-10delinsGTTTT	ENSP00000505288.1:n.10511-14_10511-10delinsGTTTT
ENST00000265104.4:c.10556-14_10556-10delinsGTTTT	ENSP00000265104.4:n.10556-14_10556-10delinsGTTTT
NM_001369.2:c.10556-14_10556-10delinsGTTTT	NP_001360.1:n.10556-14_10556-10delinsGTTTT
XM_005248262.2:c.10511-14_10511-10delinsGTTTT	XP_005248319.1:n.10511-14_10511-10delinsGTTTT
XM_005248262.3:c.10664-14_10664-10delinsGTTTT	XP_005248319.2:n.10664-14_10664-10delinsGTTTT
XM_017009177.1:c.10664-14_10664-10delinsGTTTT	XP_016864666.1:n.10664-14_10664-10delinsGTTTT
XM_017009178.1:c.9569-14_9569-10delinsGTTTT	XP_016864667.1:n.9569-14_9569-10delinsGTTTT
XM_017009179.2:c.9569-14_9569-10delinsGTTTT	XP_016864668.1:n.9569-14_9569-10delinsGTTTT
XM_017009180.1:c.10664-14_10664-10delinsGTTTT	XP_016864669.1:n.10664-14_10664-10delinsGTTTT
XM_017009181.1:c.10664-14_10664-10delinsGTTTT	XP_016864670.1:n.10664-14_10664-10delinsGTTTT
XM_017009182.1:c.10664-14_10664-10delinsGTTTT	XP_016864671.1:n.10664-14_10664-10delinsGTTTT
XM_017009185.1:c.5753-14_5753-10delinsGTTTT	XP_016864674.1:n.5753-14_5753-10delinsGTTTT
XM_017009186.1:c.5306-14_5306-10delinsGTTTT	XP_016864675.1:n.5306-14_5306-10delinsGTTTT
XM_017009188.1:c.4643-14_4643-10delinsGTTTT	XP_016864677.1:n.4643-14_4643-10delinsGTTTT
XM_024454388.1:c.9569-14_9569-10delinsGTTTT	XP_024310156.1:n.9569-14_9569-10delinsGTTTT
XM_024454389.1:c.9158-14_9158-10delinsGTTTT	XP_024310157.1:n.9158-14_9158-10delinsGTTTT
NM_001369.3:c.10556-14_10556-10delinsGTTTT MANE Select	NP_001360.1:n.10556-14_10556-10delinsGTTTT