Canonical Allele Identifier: CA443259084

Gene: DNAH5

Linked Data

• dbSNP Id: rs1170573831
• gnomAD v3: 5-13780861-A-G
• gnomAD v4: 5-13780861-A-G
• MyVariant Identifiers: chr5:g.13780970A>G (hg19) ; chr5:g.13780861A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13780861A>G , CM000667.2:g.13780861A>G	GRCh38
NC_000005.9:g.13780970A>G , CM000667.1:g.13780970A>G	GRCh37
NC_000005.8:g.13833970A>G	NCBI36
NG_013081.1:g.168620T>C
NG_013081.2:g.168620T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.8919T>C MANE Select	ENSP00000265104.4:p.Ala2973=
ENST00000681290.1:c.8874T>C	ENSP00000505288.1:p.Ala2958=
ENST00000265104.4:c.8919T>C	ENSP00000265104.4:p.Ala2973=
NM_001369.2:c.8919T>C	NP_001360.1:p.Ala2973=
XM_005248262.2:c.8874T>C	XP_005248319.1:p.Ala2958=
XM_011513990.1:c.8919T>C	XP_011512292.1:p.Ala2973=
XR_925598.1:n.9028-3506T>C
XM_005248262.3:c.9027T>C	XP_005248319.2:p.Ala3009=
XM_017009177.1:c.9027T>C	XP_016864666.1:p.Ala3009=
XM_017009178.1:c.7932T>C	XP_016864667.1:p.Ala2644=
XM_017009179.2:c.7932T>C	XP_016864668.1:p.Ala2644=
XM_017009180.1:c.9027T>C	XP_016864669.1:p.Ala3009=
XM_017009181.1:c.9027T>C	XP_016864670.1:p.Ala3009=
XM_017009182.1:c.9027T>C	XP_016864671.1:p.Ala3009=
XM_017009183.1:c.9027T>C	XP_016864672.1:p.Ala3009=
XM_017009184.1:c.9027T>C	XP_016864673.1:p.Ala3009=
XM_017009185.1:c.4116T>C	XP_016864674.1:p.Ala1372=
XM_017009186.1:c.3669T>C	XP_016864675.1:p.Ala1223=
XM_017009188.1:c.3006T>C	XP_016864677.1:p.Ala1002=
XM_024454388.1:c.7932T>C	XP_024310156.1:p.Ala2644=
XM_024454389.1:c.7521T>C	XP_024310157.1:p.Ala2507=
XR_001742034.1:n.8946-3506T>C
XR_001742035.1:n.8946-3506T>C
NM_001369.3:c.8919T>C MANE Select	NP_001360.1:p.Ala2973=