Canonical Allele Identifier: CA359197449

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13708256-C-T
• MyVariant Identifiers: chr5:g.13708365C>T (hg19) ; chr5:g.13708256C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708256C>T , CM000667.2:g.13708256C>T	GRCh38
NC_000005.9:g.13708365C>T , CM000667.1:g.13708365C>T	GRCh37
NC_000005.8:g.13761365C>T	NCBI36
NG_013081.1:g.241225G>A
NG_013081.2:g.241225G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.538G>A
ENST00000265104.5:c.13205G>A MANE Select	ENSP00000265104.4:p.Arg4402Lys
ENST00000681290.1:c.13160G>A	ENSP00000505288.1:p.Arg4387Lys
ENST00000265104.4:c.13205G>A	ENSP00000265104.4:p.Arg4402Lys
NM_001369.2:c.13205G>A	NP_001360.1:p.Arg4402Lys
XM_005248262.2:c.13160G>A	XP_005248319.1:p.Arg4387Lys
XM_005248262.3:c.13313G>A	XP_005248319.2:p.Arg4438Lys
XM_017009177.1:c.12893G>A	XP_016864666.1:p.Arg4298Lys
XM_017009178.1:c.12218G>A	XP_016864667.1:p.Arg4073Lys
XM_017009179.2:c.12218G>A	XP_016864668.1:p.Arg4073Lys
XM_017009185.1:c.8402G>A	XP_016864674.1:p.Arg2801Lys
XM_017009186.1:c.7955G>A	XP_016864675.1:p.Arg2652Lys
XM_017009188.1:c.7292G>A	XP_016864677.1:p.Arg2431Lys
XM_024454388.1:c.12218G>A	XP_024310156.1:p.Arg4073Lys
XM_024454389.1:c.11807G>A	XP_024310157.1:p.Arg3936Lys
NM_001369.3:c.13205G>A MANE Select	NP_001360.1:p.Arg4402Lys