Canonical Allele Identifier: CA1528407741

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13718980G= , CM000667.2:g.13718980G=	GRCh38
NC_000005.9:g.13719089G= , CM000667.1:g.13719089G=	GRCh37
NC_000005.8:g.13772089G=	NCBI36
NG_013081.1:g.230501C=
NG_013081.2:g.230501C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001369.3:c.12401C= MANE Select	NP_001360.1:p.Ala4134=
ENST00000265104.5:c.12401C= MANE Select	ENSP00000265104.4:p.Ala4134=
NM_001369.2:c.12401C=	NP_001360.1:p.Ala4134=
ENST00000265104.4:c.12401C=	ENSP00000265104.4:p.Ala4134=
ENST00000681290.1:c.12356C=	ENSP00000505288.1:p.Ala4119=
XM_005248262.2:c.12356C=	XP_005248319.1:p.Ala4119=
XM_005248262.3:c.12509C=	XP_005248319.2:p.Ala4170=
XM_017009177.1:c.12509C=	XP_016864666.1:p.Ala4170=
XM_017009178.1:c.11414C=	XP_016864667.1:p.Ala3805=
XM_017009179.2:c.11414C=	XP_016864668.1:p.Ala3805=
XM_017009180.1:c.12509C=	XP_016864669.1:p.Ala4170=
XM_017009185.1:c.7598C=	XP_016864674.1:p.Ala2533=
XM_017009186.1:c.7151C=	XP_016864675.1:p.Ala2384=
XM_017009188.1:c.6488C=	XP_016864677.1:p.Ala2163=
XM_024454388.1:c.11414C=	XP_024310156.1:p.Ala3805=
XM_024454389.1:c.11003C=	XP_024310157.1:p.Ala3668=