Canonical Allele Identifier: CA1528407032

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717405C= , CM000667.2:g.13717405C=	GRCh38
NC_000005.9:g.13717514C= , CM000667.1:g.13717514C=	GRCh37
NC_000005.8:g.13770514C=	NCBI36
NG_013081.1:g.232076G=
NG_013081.2:g.232076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.12615G= MANE Select	ENSP00000265104.4:p.Gly4205=
ENST00000681290.1:c.12570G=	ENSP00000505288.1:p.Gly4190=
ENST00000265104.4:c.12615G=	ENSP00000265104.4:p.Gly4205=
NM_001369.2:c.12615G=	NP_001360.1:p.Gly4205=
XM_005248262.2:c.12570G=	XP_005248319.1:p.Gly4190=
XM_005248262.3:c.12723G=	XP_005248319.2:p.Gly4241=
XM_017009177.1:c.12723G=	XP_016864666.1:p.Gly4241=
XM_017009178.1:c.11628G=	XP_016864667.1:p.Gly3876=
XM_017009179.2:c.11628G=	XP_016864668.1:p.Gly3876=
XM_017009180.1:c.12723G=	XP_016864669.1:p.Gly4241=
XM_017009185.1:c.7812G=	XP_016864674.1:p.Gly2604=
XM_017009186.1:c.7365G=	XP_016864675.1:p.Gly2455=
XM_017009188.1:c.6702G=	XP_016864677.1:p.Gly2234=
XM_024454388.1:c.11628G=	XP_024310156.1:p.Gly3876=
XM_024454389.1:c.11217G=	XP_024310157.1:p.Gly3739=
NM_001369.3:c.12615G= MANE Select	NP_001360.1:p.Gly4205=