Canonical Allele Identifier: CA3201631

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13718909G>A , CM000667.2:g.13718909G>A	GRCh38
NC_000005.9:g.13719018G>A , CM000667.1:g.13719018G>A	GRCh37
NC_000005.8:g.13772018G>A	NCBI36
NG_013081.1:g.230572C>T
NG_013081.2:g.230572C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.12472C>T MANE Select	NP_001360.1:p.Arg4158Trp
ENST00000265104.5:c.12472C>T MANE Select	ENSP00000265104.4:p.Arg4158Trp
NM_001369.2:c.12472C>T	NP_001360.1:p.Arg4158Trp
ENST00000265104.4:c.12472C>T	ENSP00000265104.4:p.Arg4158Trp
ENST00000681290.1:c.12427C>T	ENSP00000505288.1:p.Arg4143Trp
XM_005248262.2:c.12427C>T	XP_005248319.1:p.Arg4143Trp
XM_005248262.3:c.12580C>T	XP_005248319.2:p.Arg4194Trp
XM_017009177.1:c.12580C>T	XP_016864666.1:p.Arg4194Trp
XM_017009178.1:c.11485C>T	XP_016864667.1:p.Arg3829Trp
XM_017009179.2:c.11485C>T	XP_016864668.1:p.Arg3829Trp
XM_017009180.1:c.12580C>T	XP_016864669.1:p.Arg4194Trp
XM_017009185.1:c.7669C>T	XP_016864674.1:p.Arg2557Trp
XM_017009186.1:c.7222C>T	XP_016864675.1:p.Arg2408Trp
XM_017009188.1:c.6559C>T	XP_016864677.1:p.Arg2187Trp
XM_024454388.1:c.11485C>T	XP_024310156.1:p.Arg3829Trp
XM_024454389.1:c.11074C>T	XP_024310157.1:p.Arg3692Trp