Canonical Allele Identifier: CA443248660

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13692147C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692038C>T , CM000667.2:g.13692038C>T	GRCh38
NC_000005.9:g.13692147C>T , CM000667.1:g.13692147C>T	GRCh37
NC_000005.8:g.13745147C>T	NCBI36
NG_013081.1:g.257443G>A
NG_013081.2:g.257443G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1154G>A
ENST00000265104.5:c.13821G>A MANE Select	ENSP00000265104.4:p.Gln4607=
ENST00000681290.1:c.13776G>A	ENSP00000505288.1:p.Gln4592=
ENST00000265104.4:c.13821G>A	ENSP00000265104.4:p.Gln4607=
NM_001369.2:c.13821G>A	NP_001360.1:p.Gln4607=
XM_005248262.2:c.13776G>A	XP_005248319.1:p.Gln4592=
XM_005248262.3:c.13929G>A	XP_005248319.2:p.Gln4643=
XM_017009177.1:c.13509G>A	XP_016864666.1:p.Gln4503=
XM_017009178.1:c.12834G>A	XP_016864667.1:p.Gln4278=
XM_017009179.2:c.12834G>A	XP_016864668.1:p.Gln4278=
XM_017009185.1:c.9018G>A	XP_016864674.1:p.Gln3006=
XM_017009186.1:c.8571G>A	XP_016864675.1:p.Gln2857=
XM_017009188.1:c.7908G>A	XP_016864677.1:p.Gln2636=
XM_024454388.1:c.12834G>A	XP_024310156.1:p.Gln4278=
XM_024454389.1:c.12423G>A	XP_024310157.1:p.Gln4141=
NM_001369.3:c.13821G>A MANE Select	NP_001360.1:p.Gln4607=