Canonical Allele Identifier: CA359197627

Gene: DNAH5

Linked Data

• MyVariant Identifiers: chr5:g.13708378C>T (hg19) ; chr5:g.13708269C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13708269C>T , CM000667.2:g.13708269C>T	GRCh38
NC_000005.9:g.13708378C>T , CM000667.1:g.13708378C>T	GRCh37
NC_000005.8:g.13761378C>T	NCBI36
NG_013081.1:g.241212G>A
NG_013081.2:g.241212G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.525G>A
ENST00000265104.5:c.13192G>A MANE Select	ENSP00000265104.4:p.Asp4398Asn
ENST00000681290.1:c.13147G>A	ENSP00000505288.1:p.Asp4383Asn
ENST00000265104.4:c.13192G>A	ENSP00000265104.4:p.Asp4398Asn
NM_001369.2:c.13192G>A	NP_001360.1:p.Asp4398Asn
XM_005248262.2:c.13147G>A	XP_005248319.1:p.Asp4383Asn
XM_005248262.3:c.13300G>A	XP_005248319.2:p.Asp4434Asn
XM_017009177.1:c.12880G>A	XP_016864666.1:p.Asp4294Asn
XM_017009178.1:c.12205G>A	XP_016864667.1:p.Asp4069Asn
XM_017009179.2:c.12205G>A	XP_016864668.1:p.Asp4069Asn
XM_017009185.1:c.8389G>A	XP_016864674.1:p.Asp2797Asn
XM_017009186.1:c.7942G>A	XP_016864675.1:p.Asp2648Asn
XM_017009188.1:c.7279G>A	XP_016864677.1:p.Asp2427Asn
XM_024454388.1:c.12205G>A	XP_024310156.1:p.Asp4069Asn
XM_024454389.1:c.11794G>A	XP_024310157.1:p.Asp3932Asn
NM_001369.3:c.13192G>A MANE Select	NP_001360.1:p.Asp4398Asn