Canonical Allele Identifier: CA359213082

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13721017G>A , CM000667.2:g.13721017G>A	GRCh38
NC_000005.9:g.13721126G>A , CM000667.1:g.13721126G>A	GRCh37
NC_000005.8:g.13774126G>A	NCBI36
NG_013081.1:g.228464C>T
NG_013081.2:g.228464C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.12262C>T MANE Select	NP_001360.1:p.Gln4088Ter
ENST00000265104.5:c.12262C>T MANE Select	ENSP00000265104.4:p.Gln4088Ter
NM_001369.2:c.12262C>T	NP_001360.1:p.Gln4088Ter
ENST00000265104.4:c.12262C>T	ENSP00000265104.4:p.Gln4088Ter
ENST00000681290.1:c.12217C>T	ENSP00000505288.1:p.Gln4073Ter
XM_005248262.2:c.12217C>T	XP_005248319.1:p.Gln4073Ter
XM_005248262.3:c.12370C>T	XP_005248319.2:p.Gln4124Ter
XM_017009177.1:c.12370C>T	XP_016864666.1:p.Gln4124Ter
XM_017009178.1:c.11275C>T	XP_016864667.1:p.Gln3759Ter
XM_017009179.2:c.11275C>T	XP_016864668.1:p.Gln3759Ter
XM_017009180.1:c.12370C>T	XP_016864669.1:p.Gln4124Ter
XM_017009185.1:c.7459C>T	XP_016864674.1:p.Gln2487Ter
XM_017009186.1:c.7012C>T	XP_016864675.1:p.Gln2338Ter
XM_017009188.1:c.6349C>T	XP_016864677.1:p.Gln2117Ter
XM_024454388.1:c.11275C>T	XP_024310156.1:p.Gln3759Ter
XM_024454389.1:c.10864C>T	XP_024310157.1:p.Gln3622Ter