Canonical Allele Identifier: CA359195811

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13758941G>A , CM000667.2:g.13758941G>A	GRCh38
NC_000005.9:g.13759050G>A , CM000667.1:g.13759050G>A	GRCh37
NC_000005.8:g.13812050G>A	NCBI36
NG_013081.1:g.190540C>T
NG_013081.2:g.190540C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.10324C>T MANE Select	NP_001360.1:p.Gln3442Ter
ENST00000265104.5:c.10324C>T MANE Select	ENSP00000265104.4:p.Gln3442Ter
NM_001369.2:c.10324C>T	NP_001360.1:p.Gln3442Ter
ENST00000265104.4:c.10324C>T	ENSP00000265104.4:p.Gln3442Ter
ENST00000681290.1:c.10279C>T	ENSP00000505288.1:p.Gln3427Ter
XM_005248262.2:c.10279C>T	XP_005248319.1:p.Gln3427Ter
XM_005248262.3:c.10432C>T	XP_005248319.2:p.Gln3478Ter
XM_017009177.1:c.10432C>T	XP_016864666.1:p.Gln3478Ter
XM_017009178.1:c.9337C>T	XP_016864667.1:p.Gln3113Ter
XM_017009179.2:c.9337C>T	XP_016864668.1:p.Gln3113Ter
XM_017009180.1:c.10432C>T	XP_016864669.1:p.Gln3478Ter
XM_017009181.1:c.10432C>T	XP_016864670.1:p.Gln3478Ter
XM_017009182.1:c.10432C>T	XP_016864671.1:p.Gln3478Ter
XM_017009185.1:c.5521C>T	XP_016864674.1:p.Gln1841Ter
XM_017009186.1:c.5074C>T	XP_016864675.1:p.Gln1692Ter
XM_017009188.1:c.4411C>T	XP_016864677.1:p.Gln1471Ter
XM_024454388.1:c.9337C>T	XP_024310156.1:p.Gln3113Ter
XM_024454389.1:c.8926C>T	XP_024310157.1:p.Gln2976Ter