Canonical Allele Identifier: CA1528403836

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708384T= , CM000667.2:g.13708384T=	GRCh38
NC_000005.9:g.13708493T= , CM000667.1:g.13708493T=	GRCh37
NC_000005.8:g.13761493T=	NCBI36
NG_013081.1:g.241097A=
NG_013081.2:g.241097A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.459-49A=
ENST00000265104.5:c.13126-49A= MANE Select	ENSP00000265104.4:n.13126-49A=
ENST00000681290.1:c.13081-49A=	ENSP00000505288.1:n.13081-49A=
ENST00000265104.4:c.13126-49A=	ENSP00000265104.4:n.13126-49A=
NM_001369.2:c.13126-49A=	NP_001360.1:n.13126-49A=
XM_005248262.2:c.13081-49A=	XP_005248319.1:n.13081-49A=
XM_005248262.3:c.13234-49A=	XP_005248319.2:n.13234-49A=
XM_017009177.1:c.12814-49A=	XP_016864666.1:n.12814-49A=
XM_017009178.1:c.12139-49A=	XP_016864667.1:n.12139-49A=
XM_017009179.2:c.12139-49A=	XP_016864668.1:n.12139-49A=
XM_017009185.1:c.8323-49A=	XP_016864674.1:n.8323-49A=
XM_017009186.1:c.7876-49A=	XP_016864675.1:n.7876-49A=
XM_017009188.1:c.7213-49A=	XP_016864677.1:n.7213-49A=
XM_024454388.1:c.12139-49A=	XP_024310156.1:n.12139-49A=
XM_024454389.1:c.11728-49A=	XP_024310157.1:n.11728-49A=
NM_001369.3:c.13126-49A= MANE Select	NP_001360.1:n.13126-49A=