Canonical Allele Identifier: CA359212661

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13780965T>A (hg19) ; chr5:g.13780856T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780856T>A , CM000667.2:g.13780856T>A	GRCh38
NC_000005.9:g.13780965T>A , CM000667.1:g.13780965T>A	GRCh37
NC_000005.8:g.13833965T>A	NCBI36
NG_013081.1:g.168625A>T
NG_013081.2:g.168625A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.8924A>T MANE Select	ENSP00000265104.4:p.Tyr2975Phe
ENST00000681290.1:c.8879A>T	ENSP00000505288.1:p.Tyr2960Phe
ENST00000265104.4:c.8924A>T	ENSP00000265104.4:p.Tyr2975Phe
NM_001369.2:c.8924A>T	NP_001360.1:p.Tyr2975Phe
XM_005248262.2:c.8879A>T	XP_005248319.1:p.Tyr2960Phe
XM_011513990.1:c.8924A>T	XP_011512292.1:p.Tyr2975Phe
XR_925598.1:n.9028-3501A>T
XM_005248262.3:c.9032A>T	XP_005248319.2:p.Tyr3011Phe
XM_017009177.1:c.9032A>T	XP_016864666.1:p.Tyr3011Phe
XM_017009178.1:c.7937A>T	XP_016864667.1:p.Tyr2646Phe
XM_017009179.2:c.7937A>T	XP_016864668.1:p.Tyr2646Phe
XM_017009180.1:c.9032A>T	XP_016864669.1:p.Tyr3011Phe
XM_017009181.1:c.9032A>T	XP_016864670.1:p.Tyr3011Phe
XM_017009182.1:c.9032A>T	XP_016864671.1:p.Tyr3011Phe
XM_017009183.1:c.9032A>T	XP_016864672.1:p.Tyr3011Phe
XM_017009184.1:c.9032A>T	XP_016864673.1:p.Tyr3011Phe
XM_017009185.1:c.4121A>T	XP_016864674.1:p.Tyr1374Phe
XM_017009186.1:c.3674A>T	XP_016864675.1:p.Tyr1225Phe
XM_017009188.1:c.3011A>T	XP_016864677.1:p.Tyr1004Phe
XM_024454388.1:c.7937A>T	XP_024310156.1:p.Tyr2646Phe
XM_024454389.1:c.7526A>T	XP_024310157.1:p.Tyr2509Phe
XR_001742034.1:n.8946-3501A>T
XR_001742035.1:n.8946-3501A>T
NM_001369.3:c.8924A>T MANE Select	NP_001360.1:p.Tyr2975Phe