Canonical Allele Identifier: CA359190086

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13752316A>T (hg19) ; chr5:g.13752207A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752207A>T , CM000667.2:g.13752207A>T	GRCh38
NC_000005.9:g.13752316A>T , CM000667.1:g.13752316A>T	GRCh37
NC_000005.8:g.13805316A>T	NCBI36
NG_013081.1:g.197274T>A
NG_013081.2:g.197274T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10955T>A MANE Select	ENSP00000265104.4:p.Val3652Asp
ENST00000681290.1:c.10910T>A	ENSP00000505288.1:p.Val3637Asp
ENST00000265104.4:c.10955T>A	ENSP00000265104.4:p.Val3652Asp
NM_001369.2:c.10955T>A	NP_001360.1:p.Val3652Asp
XM_005248262.2:c.10910T>A	XP_005248319.1:p.Val3637Asp
XM_005248262.3:c.11063T>A	XP_005248319.2:p.Val3688Asp
XM_017009177.1:c.11063T>A	XP_016864666.1:p.Val3688Asp
XM_017009178.1:c.9968T>A	XP_016864667.1:p.Val3323Asp
XM_017009179.2:c.9968T>A	XP_016864668.1:p.Val3323Asp
XM_017009180.1:c.11063T>A	XP_016864669.1:p.Val3688Asp
XM_017009181.1:c.11063T>A	XP_016864670.1:p.Val3688Asp
XM_017009182.1:c.11063T>A	XP_016864671.1:p.Val3688Asp
XM_017009185.1:c.6152T>A	XP_016864674.1:p.Val2051Asp
XM_017009186.1:c.5705T>A	XP_016864675.1:p.Val1902Asp
XM_017009188.1:c.5042T>A	XP_016864677.1:p.Val1681Asp
XM_024454388.1:c.9968T>A	XP_024310156.1:p.Val3323Asp
XM_024454389.1:c.9557T>A	XP_024310157.1:p.Val3186Asp
NM_001369.3:c.10955T>A MANE Select	NP_001360.1:p.Val3652Asp