Canonical Allele Identifier: CA359211823

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13841931A>G (hg19) ; chr5:g.13841822A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841822A>G , CM000667.2:g.13841822A>G	GRCh38
NC_000005.9:g.13841931A>G , CM000667.1:g.13841931A>G	GRCh37
NC_000005.8:g.13894931A>G	NCBI36
NG_013081.1:g.107659T>C
NG_013081.2:g.107659T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5354T>C MANE Select	ENSP00000265104.4:p.Val1785Ala
ENST00000681290.1:c.5309T>C	ENSP00000505288.1:p.Val1770Ala
ENST00000265104.4:c.5354T>C	ENSP00000265104.4:p.Val1785Ala
NM_001369.2:c.5354T>C	NP_001360.1:p.Val1785Ala
XM_005248262.2:c.5309T>C	XP_005248319.1:p.Val1770Ala
XM_011513990.1:c.5354T>C	XP_011512292.1:p.Val1785Ala
XR_925598.1:n.5561T>C
XM_005248262.3:c.5462T>C	XP_005248319.2:p.Val1821Ala
XM_017009177.1:c.5462T>C	XP_016864666.1:p.Val1821Ala
XM_017009178.1:c.4367T>C	XP_016864667.1:p.Val1456Ala
XM_017009179.2:c.4367T>C	XP_016864668.1:p.Val1456Ala
XM_017009180.1:c.5462T>C	XP_016864669.1:p.Val1821Ala
XM_017009181.1:c.5462T>C	XP_016864670.1:p.Val1821Ala
XM_017009182.1:c.5462T>C	XP_016864671.1:p.Val1821Ala
XM_017009183.1:c.5462T>C	XP_016864672.1:p.Val1821Ala
XM_017009184.1:c.5462T>C	XP_016864673.1:p.Val1821Ala
XM_017009185.1:c.551T>C	XP_016864674.1:p.Val184Ala
XM_017009186.1:c.104T>C	XP_016864675.1:p.Val35Ala
XM_017009187.1:c.5462T>C	XP_016864676.1:p.Val1821Ala
XM_024454388.1:c.4367T>C	XP_024310156.1:p.Val1456Ala
XM_024454389.1:c.3956T>C	XP_024310157.1:p.Val1319Ala
XR_001742034.1:n.5479T>C
XR_001742035.1:n.5479T>C
NM_001369.3:c.5354T>C MANE Select	NP_001360.1:p.Val1785Ala