Canonical Allele Identifier: CA443535734

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13771028C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770919C>G , CM000667.2:g.13770919C>G	GRCh38
NC_000005.9:g.13771028C>G , CM000667.1:g.13771028C>G	GRCh37
NC_000005.8:g.13824028C>G	NCBI36
NG_013081.1:g.178562G>C
NG_013081.2:g.178562G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9435G>C MANE Select	ENSP00000265104.4:p.Val3145=
ENST00000681290.1:c.9390G>C	ENSP00000505288.1:p.Val3130=
ENST00000265104.4:c.9435G>C	ENSP00000265104.4:p.Val3145=
ENST00000504001.3:n.147G>C
NM_001369.2:c.9435G>C	NP_001360.1:p.Val3145=
XM_005248262.2:c.9390G>C	XP_005248319.1:p.Val3130=
XM_005248262.3:c.9543G>C	XP_005248319.2:p.Val3181=
XM_017009177.1:c.9543G>C	XP_016864666.1:p.Val3181=
XM_017009178.1:c.8448G>C	XP_016864667.1:p.Val2816=
XM_017009179.2:c.8448G>C	XP_016864668.1:p.Val2816=
XM_017009180.1:c.9543G>C	XP_016864669.1:p.Val3181=
XM_017009181.1:c.9543G>C	XP_016864670.1:p.Val3181=
XM_017009182.1:c.9543G>C	XP_016864671.1:p.Val3181=
XM_017009183.1:c.9543G>C	XP_016864672.1:p.Val3181=
XM_017009185.1:c.4632G>C	XP_016864674.1:p.Val1544=
XM_017009186.1:c.4185G>C	XP_016864675.1:p.Val1395=
XM_017009188.1:c.3522G>C	XP_016864677.1:p.Val1174=
XM_024454388.1:c.8448G>C	XP_024310156.1:p.Val2816=
XM_024454389.1:c.8037G>C	XP_024310157.1:p.Val2679=
NM_001369.3:c.9435G>C MANE Select	NP_001360.1:p.Val3145=