Canonical Allele Identifier: CA359211839

Gene: DNAH5

Linked Data

• dbSNP Id: rs1285373457
• gnomAD v2: 5-13841935-T-G
• gnomAD v4: 5-13841826-T-G
• MyVariant Identifiers: chr5:g.13841935T>G (hg19) ; chr5:g.13841826T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13841826T>G , CM000667.2:g.13841826T>G	GRCh38
NC_000005.9:g.13841935T>G , CM000667.1:g.13841935T>G	GRCh37
NC_000005.8:g.13894935T>G	NCBI36
NG_013081.1:g.107655A>C
NG_013081.2:g.107655A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.5350A>C MANE Select	ENSP00000265104.4:p.Asn1784His
ENST00000681290.1:c.5305A>C	ENSP00000505288.1:p.Asn1769His
ENST00000265104.4:c.5350A>C	ENSP00000265104.4:p.Asn1784His
NM_001369.2:c.5350A>C	NP_001360.1:p.Asn1784His
XM_005248262.2:c.5305A>C	XP_005248319.1:p.Asn1769His
XM_011513990.1:c.5350A>C	XP_011512292.1:p.Asn1784His
XR_925598.1:n.5557A>C
XM_005248262.3:c.5458A>C	XP_005248319.2:p.Asn1820His
XM_017009177.1:c.5458A>C	XP_016864666.1:p.Asn1820His
XM_017009178.1:c.4363A>C	XP_016864667.1:p.Asn1455His
XM_017009179.2:c.4363A>C	XP_016864668.1:p.Asn1455His
XM_017009180.1:c.5458A>C	XP_016864669.1:p.Asn1820His
XM_017009181.1:c.5458A>C	XP_016864670.1:p.Asn1820His
XM_017009182.1:c.5458A>C	XP_016864671.1:p.Asn1820His
XM_017009183.1:c.5458A>C	XP_016864672.1:p.Asn1820His
XM_017009184.1:c.5458A>C	XP_016864673.1:p.Asn1820His
XM_017009185.1:c.547A>C	XP_016864674.1:p.Asn183His
XM_017009186.1:c.100A>C	XP_016864675.1:p.Asn34His
XM_017009187.1:c.5458A>C	XP_016864676.1:p.Asn1820His
XM_024454388.1:c.4363A>C	XP_024310156.1:p.Asn1455His
XM_024454389.1:c.3952A>C	XP_024310157.1:p.Asn1318His
XR_001742034.1:n.5475A>C
XR_001742035.1:n.5475A>C
NM_001369.3:c.5350A>C MANE Select	NP_001360.1:p.Asn1784His