Canonical Allele Identifier: CA3202131

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13753270A>T , CM000667.2:g.13753270A>T	GRCh38
NC_000005.9:g.13753379A>T , CM000667.1:g.13753379A>T	GRCh37
NC_000005.8:g.13806379A>T	NCBI36
NG_013081.1:g.196211T>A
NG_013081.2:g.196211T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.10835T>A MANE Select	NP_001360.1:p.Ile3612Asn
ENST00000265104.5:c.10835T>A MANE Select	ENSP00000265104.4:p.Ile3612Asn
NM_001369.2:c.10835T>A	NP_001360.1:p.Ile3612Asn
ENST00000265104.4:c.10835T>A	ENSP00000265104.4:p.Ile3612Asn
ENST00000681290.1:c.10790T>A	ENSP00000505288.1:p.Ile3597Asn
XM_005248262.2:c.10790T>A	XP_005248319.1:p.Ile3597Asn
XM_005248262.3:c.10943T>A	XP_005248319.2:p.Ile3648Asn
XM_017009177.1:c.10943T>A	XP_016864666.1:p.Ile3648Asn
XM_017009178.1:c.9848T>A	XP_016864667.1:p.Ile3283Asn
XM_017009179.2:c.9848T>A	XP_016864668.1:p.Ile3283Asn
XM_017009180.1:c.10943T>A	XP_016864669.1:p.Ile3648Asn
XM_017009181.1:c.10943T>A	XP_016864670.1:p.Ile3648Asn
XM_017009182.1:c.10943T>A	XP_016864671.1:p.Ile3648Asn
XM_017009185.1:c.6032T>A	XP_016864674.1:p.Ile2011Asn
XM_017009186.1:c.5585T>A	XP_016864675.1:p.Ile1862Asn
XM_017009188.1:c.4922T>A	XP_016864677.1:p.Ile1641Asn
XM_024454388.1:c.9848T>A	XP_024310156.1:p.Ile3283Asn
XM_024454389.1:c.9437T>A	XP_024310157.1:p.Ile3146Asn