Canonical Allele Identifier: CA1528399780

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13701060A= , CM000667.2:g.13701060A=	GRCh38
NC_000005.9:g.13701169A= , CM000667.1:g.13701169A=	GRCh37
NC_000005.8:g.13754169A=	NCBI36
NG_013081.1:g.248421T=
NG_013081.2:g.248421T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.825-189T=
ENST00000265104.5:c.13492-189T= MANE Select	ENSP00000265104.4:n.13492-189T=
ENST00000681290.1:c.13447-189T=	ENSP00000505288.1:n.13447-189T=
ENST00000265104.4:c.13492-189T=	ENSP00000265104.4:n.13492-189T=
NM_001369.2:c.13492-189T=	NP_001360.1:n.13492-189T=
XM_005248262.2:c.13447-189T=	XP_005248319.1:n.13447-189T=
XM_005248262.3:c.13600-189T=	XP_005248319.2:n.13600-189T=
XM_017009177.1:c.13180-189T=	XP_016864666.1:n.13180-189T=
XM_017009178.1:c.12505-189T=	XP_016864667.1:n.12505-189T=
XM_017009179.2:c.12505-189T=	XP_016864668.1:n.12505-189T=
XM_017009185.1:c.8689-189T=	XP_016864674.1:n.8689-189T=
XM_017009186.1:c.8242-189T=	XP_016864675.1:n.8242-189T=
XM_017009188.1:c.7579-189T=	XP_016864677.1:n.7579-189T=
XM_024454388.1:c.12505-189T=	XP_024310156.1:n.12505-189T=
XM_024454389.1:c.12094-189T=	XP_024310157.1:n.12094-189T=
NM_001369.3:c.13492-189T= MANE Select	NP_001360.1:n.13492-189T=