Canonical Allele Identifier: CA1528395656

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13691591G= , CM000667.2:g.13691591G=	GRCh38
NC_000005.9:g.13691700G= , CM000667.1:g.13691700G=	GRCh37
NC_000005.8:g.13744700G=	NCBI36
NG_013081.1:g.257890C=
NG_013081.2:g.257890C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1601C=
ENST00000265104.5:c.*393C= MANE Select	ENSP00000265104.4:n.*393C=
ENST00000681290.1:c.*393C=	ENSP00000505288.1:n.*393C=
ENST00000265104.4:c.*393C=	ENSP00000265104.4:n.*393C=
NM_001369.2:c.*393C=	NP_001360.1:n.*393C=
XM_005248262.2:c.*393C=	XP_005248319.1:n.*393C=
XM_005248262.3:c.*393C=	XP_005248319.2:n.*393C=
XM_017009177.1:c.*393C=	XP_016864666.1:n.*393C=
XM_017009178.1:c.*393C=	XP_016864667.1:n.*393C=
XM_017009179.2:c.*393C=	XP_016864668.1:n.*393C=
XM_017009185.1:c.*393C=	XP_016864674.1:n.*393C=
XM_017009186.1:c.*393C=	XP_016864675.1:n.*393C=
XM_017009188.1:c.*393C=	XP_016864677.1:n.*393C=
XM_024454388.1:c.*393C=	XP_024310156.1:n.*393C=
XM_024454389.1:c.*393C=	XP_024310157.1:n.*393C=
NM_001369.3:c.*393C= MANE Select	NP_001360.1:n.*393C=