Canonical Allele Identifier: CA359197387

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708362A>T (hg19) ; chr5:g.13708253A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708253A>T , CM000667.2:g.13708253A>T	GRCh38
NC_000005.9:g.13708362A>T , CM000667.1:g.13708362A>T	GRCh37
NC_000005.8:g.13761362A>T	NCBI36
NG_013081.1:g.241228T>A
NG_013081.2:g.241228T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.541T>A
ENST00000265104.5:c.13208T>A MANE Select	ENSP00000265104.4:p.Val4403Glu
ENST00000681290.1:c.13163T>A	ENSP00000505288.1:p.Val4388Glu
ENST00000265104.4:c.13208T>A	ENSP00000265104.4:p.Val4403Glu
NM_001369.2:c.13208T>A	NP_001360.1:p.Val4403Glu
XM_005248262.2:c.13163T>A	XP_005248319.1:p.Val4388Glu
XM_005248262.3:c.13316T>A	XP_005248319.2:p.Val4439Glu
XM_017009177.1:c.12896T>A	XP_016864666.1:p.Val4299Glu
XM_017009178.1:c.12221T>A	XP_016864667.1:p.Val4074Glu
XM_017009179.2:c.12221T>A	XP_016864668.1:p.Val4074Glu
XM_017009185.1:c.8405T>A	XP_016864674.1:p.Val2802Glu
XM_017009186.1:c.7958T>A	XP_016864675.1:p.Val2653Glu
XM_017009188.1:c.7295T>A	XP_016864677.1:p.Val2432Glu
XM_024454388.1:c.12221T>A	XP_024310156.1:p.Val4074Glu
XM_024454389.1:c.11810T>A	XP_024310157.1:p.Val3937Glu
NM_001369.3:c.13208T>A MANE Select	NP_001360.1:p.Val4403Glu