Canonical Allele Identifier: CA1528406992

Gene: DNAH5

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13717304C= , CM000667.2:g.13717304C=	GRCh38
NC_000005.9:g.13717413C= , CM000667.1:g.13717413C=	GRCh37
NC_000005.8:g.13770413C=	NCBI36
NG_013081.1:g.232177G=
NG_013081.2:g.232177G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.12705+11G= MANE Select	ENSP00000265104.4:n.12705+11G=
ENST00000681290.1:c.12660+11G=	ENSP00000505288.1:n.12660+11G=
ENST00000265104.4:c.12705+11G=	ENSP00000265104.4:n.12705+11G=
NM_001369.2:c.12705+11G=	NP_001360.1:n.12705+11G=
XM_005248262.2:c.12660+11G=	XP_005248319.1:n.12660+11G=
XM_005248262.3:c.12813+11G=	XP_005248319.2:n.12813+11G=
XM_017009177.1:c.12813+11G=	XP_016864666.1:n.12813+11G=
XM_017009178.1:c.11718+11G=	XP_016864667.1:n.11718+11G=
XM_017009179.2:c.11718+11G=	XP_016864668.1:n.11718+11G=
XM_017009180.1:c.12813+11G=	XP_016864669.1:n.12813+11G=
XM_017009185.1:c.7902+11G=	XP_016864674.1:n.7902+11G=
XM_017009186.1:c.7455+11G=	XP_016864675.1:n.7455+11G=
XM_017009188.1:c.6792+11G=	XP_016864677.1:n.6792+11G=
XM_024454388.1:c.11718+11G=	XP_024310156.1:n.11718+11G=
XM_024454389.1:c.11307+11G=	XP_024310157.1:n.11307+11G=
NM_001369.3:c.12705+11G= MANE Select	NP_001360.1:n.12705+11G=