Canonical Allele Identifier: CA359202559

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13830769A>G (hg19) ; chr5:g.13830660A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13830660A>G , CM000667.2:g.13830660A>G	GRCh38
NC_000005.9:g.13830769A>G , CM000667.1:g.13830769A>G	GRCh37
NC_000005.8:g.13883769A>G	NCBI36
NG_013081.1:g.118821T>C
NG_013081.2:g.118821T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.929T>C
ENST00000265104.5:c.5998T>C MANE Select	ENSP00000265104.4:p.Tyr2000His
ENST00000681290.1:c.5953T>C	ENSP00000505288.1:p.Tyr1985His
ENST00000265104.4:c.5998T>C	ENSP00000265104.4:p.Tyr2000His
NM_001369.2:c.5998T>C	NP_001360.1:p.Tyr2000His
XM_005248262.2:c.5953T>C	XP_005248319.1:p.Tyr1985His
XM_011513990.1:c.5998T>C	XP_011512292.1:p.Tyr2000His
XR_925598.1:n.6205T>C
XM_005248262.3:c.6106T>C	XP_005248319.2:p.Tyr2036His
XM_017009177.1:c.6106T>C	XP_016864666.1:p.Tyr2036His
XM_017009178.1:c.5011T>C	XP_016864667.1:p.Tyr1671His
XM_017009179.2:c.5011T>C	XP_016864668.1:p.Tyr1671His
XM_017009180.1:c.6106T>C	XP_016864669.1:p.Tyr2036His
XM_017009181.1:c.6106T>C	XP_016864670.1:p.Tyr2036His
XM_017009182.1:c.6106T>C	XP_016864671.1:p.Tyr2036His
XM_017009183.1:c.6106T>C	XP_016864672.1:p.Tyr2036His
XM_017009184.1:c.6106T>C	XP_016864673.1:p.Tyr2036His
XM_017009185.1:c.1195T>C	XP_016864674.1:p.Tyr399His
XM_017009186.1:c.748T>C	XP_016864675.1:p.Tyr250His
XM_017009187.1:c.6106T>C	XP_016864676.1:p.Tyr2036His
XM_017009188.1:c.85T>C	XP_016864677.1:p.Tyr29His
XM_024454388.1:c.5011T>C	XP_024310156.1:p.Tyr1671His
XM_024454389.1:c.4600T>C	XP_024310157.1:p.Tyr1534His
XR_001742034.1:n.6123T>C
XR_001742035.1:n.6123T>C
NM_001369.3:c.5998T>C MANE Select	NP_001360.1:p.Tyr2000His