Canonical Allele Identifier: CA1528422925

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752163T= , CM000667.2:g.13752163T=	GRCh38
NC_000005.9:g.13752272T= , CM000667.1:g.13752272T=	GRCh37
NC_000005.8:g.13805272T=	NCBI36
NG_013081.1:g.197318A=
NG_013081.2:g.197318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10999A= MANE Select	ENSP00000265104.4:p.Asn3667=
ENST00000681290.1:c.10954A=	ENSP00000505288.1:p.Asn3652=
ENST00000265104.4:c.10999A=	ENSP00000265104.4:p.Asn3667=
NM_001369.2:c.10999A=	NP_001360.1:p.Asn3667=
XM_005248262.2:c.10954A=	XP_005248319.1:p.Asn3652=
XM_005248262.3:c.11107A=	XP_005248319.2:p.Asn3703=
XM_017009177.1:c.11107A=	XP_016864666.1:p.Asn3703=
XM_017009178.1:c.10012A=	XP_016864667.1:p.Asn3338=
XM_017009179.2:c.10012A=	XP_016864668.1:p.Asn3338=
XM_017009180.1:c.11107A=	XP_016864669.1:p.Asn3703=
XM_017009181.1:c.11107A=	XP_016864670.1:p.Asn3703=
XM_017009182.1:c.11107A=	XP_016864671.1:p.Asn3703=
XM_017009185.1:c.6196A=	XP_016864674.1:p.Asn2066=
XM_017009186.1:c.5749A=	XP_016864675.1:p.Asn1917=
XM_017009188.1:c.5086A=	XP_016864677.1:p.Asn1696=
XM_024454388.1:c.10012A=	XP_024310156.1:p.Asn3338=
XM_024454389.1:c.9601A=	XP_024310157.1:p.Asn3201=
NM_001369.3:c.10999A= MANE Select	NP_001360.1:p.Asn3667=