Canonical Allele Identifier: CA1528408625

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13720917T= , CM000667.2:g.13720917T=	GRCh38
NC_000005.9:g.13721026T= , CM000667.1:g.13721026T=	GRCh37
NC_000005.8:g.13774026T=	NCBI36
NG_013081.1:g.228564A=
NG_013081.2:g.228564A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12279+83A= MANE Select	ENSP00000265104.4:n.12279+83A=
ENST00000681290.1:c.12234+83A=	ENSP00000505288.1:n.12234+83A=
ENST00000265104.4:c.12279+83A=	ENSP00000265104.4:n.12279+83A=
NM_001369.2:c.12279+83A=	NP_001360.1:n.12279+83A=
XM_005248262.2:c.12234+83A=	XP_005248319.1:n.12234+83A=
XM_005248262.3:c.12387+83A=	XP_005248319.2:n.12387+83A=
XM_017009177.1:c.12387+83A=	XP_016864666.1:n.12387+83A=
XM_017009178.1:c.11292+83A=	XP_016864667.1:n.11292+83A=
XM_017009179.2:c.11292+83A=	XP_016864668.1:n.11292+83A=
XM_017009180.1:c.12387+83A=	XP_016864669.1:n.12387+83A=
XM_017009185.1:c.7476+83A=	XP_016864674.1:n.7476+83A=
XM_017009186.1:c.7029+83A=	XP_016864675.1:n.7029+83A=
XM_017009188.1:c.6366+83A=	XP_016864677.1:n.6366+83A=
XM_024454388.1:c.11292+83A=	XP_024310156.1:n.11292+83A=
XM_024454389.1:c.10881+83A=	XP_024310157.1:n.10881+83A=
NM_001369.3:c.12279+83A= MANE Select	NP_001360.1:n.12279+83A=