Canonical Allele Identifier: CA113931330

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769527G>A , CM000667.2:g.13769527G>A	GRCh38
NC_000005.9:g.13769636G>A , CM000667.1:g.13769636G>A	GRCh37
NC_000005.8:g.13822636G>A	NCBI36
NG_013081.1:g.179954C>T
NG_013081.2:g.179954C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.9694C>T MANE Select	NP_001360.1:p.Gln3232Ter
ENST00000265104.5:c.9694C>T MANE Select	ENSP00000265104.4:p.Gln3232Ter
NM_001369.2:c.9694C>T	NP_001360.1:p.Gln3232Ter
ENST00000265104.4:c.9694C>T	ENSP00000265104.4:p.Gln3232Ter
ENST00000504001.3:n.406C>T
ENST00000681290.1:c.9649C>T	ENSP00000505288.1:p.Gln3217Ter
XM_005248262.2:c.9649C>T	XP_005248319.1:p.Gln3217Ter
XM_005248262.3:c.9802C>T	XP_005248319.2:p.Gln3268Ter
XM_017009177.1:c.9802C>T	XP_016864666.1:p.Gln3268Ter
XM_017009178.1:c.8707C>T	XP_016864667.1:p.Gln2903Ter
XM_017009179.2:c.8707C>T	XP_016864668.1:p.Gln2903Ter
XM_017009180.1:c.9802C>T	XP_016864669.1:p.Gln3268Ter
XM_017009181.1:c.9802C>T	XP_016864670.1:p.Gln3268Ter
XM_017009182.1:c.9802C>T	XP_016864671.1:p.Gln3268Ter
XM_017009185.1:c.4891C>T	XP_016864674.1:p.Gln1631Ter
XM_017009186.1:c.4444C>T	XP_016864675.1:p.Gln1482Ter
XM_017009188.1:c.3781C>T	XP_016864677.1:p.Gln1261Ter
XM_024454388.1:c.8707C>T	XP_024310156.1:p.Gln2903Ter
XM_024454389.1:c.8296C>T	XP_024310157.1:p.Gln2766Ter