Canonical Allele Identifier: CA443535721

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13771025G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770916G>T , CM000667.2:g.13770916G>T	GRCh38
NC_000005.9:g.13771025G>T , CM000667.1:g.13771025G>T	GRCh37
NC_000005.8:g.13824025G>T	NCBI36
NG_013081.1:g.178565C>A
NG_013081.2:g.178565C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9438C>A MANE Select	ENSP00000265104.4:p.Val3146=
ENST00000681290.1:c.9393C>A	ENSP00000505288.1:p.Val3131=
ENST00000265104.4:c.9438C>A	ENSP00000265104.4:p.Val3146=
ENST00000504001.3:n.150C>A
NM_001369.2:c.9438C>A	NP_001360.1:p.Val3146=
XM_005248262.2:c.9393C>A	XP_005248319.1:p.Val3131=
XM_005248262.3:c.9546C>A	XP_005248319.2:p.Val3182=
XM_017009177.1:c.9546C>A	XP_016864666.1:p.Val3182=
XM_017009178.1:c.8451C>A	XP_016864667.1:p.Val2817=
XM_017009179.2:c.8451C>A	XP_016864668.1:p.Val2817=
XM_017009180.1:c.9546C>A	XP_016864669.1:p.Val3182=
XM_017009181.1:c.9546C>A	XP_016864670.1:p.Val3182=
XM_017009182.1:c.9546C>A	XP_016864671.1:p.Val3182=
XM_017009183.1:c.9546C>A	XP_016864672.1:p.Val3182=
XM_017009185.1:c.4635C>A	XP_016864674.1:p.Val1545=
XM_017009186.1:c.4188C>A	XP_016864675.1:p.Val1396=
XM_017009188.1:c.3525C>A	XP_016864677.1:p.Val1175=
XM_024454388.1:c.8451C>A	XP_024310156.1:p.Val2817=
XM_024454389.1:c.8040C>A	XP_024310157.1:p.Val2680=
NM_001369.3:c.9438C>A MANE Select	NP_001360.1:p.Val3146=