Canonical Allele Identifier: CA557876740

Gene: DNAH5

Linked Data

• dbSNP Id: rs965456284
• gnomAD v2: 5-13870855-G-A
• MyVariant Identifiers: chr5:g.13870855G>A (hg19) ; chr5:g.13870746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13870746G>A , CM000667.2:g.13870746G>A	GRCh38
NC_000005.9:g.13870855G>A , CM000667.1:g.13870855G>A	GRCh37
NC_000005.8:g.13923855G>A	NCBI36
NG_013081.1:g.78735C>T
NG_013081.2:g.78735C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265104.5:c.3834+21C>T MANE Select	ENSP00000265104.4:n.3834+21C>T
ENST00000681290.1:c.3789+21C>T	ENSP00000505288.1:n.3789+21C>T
ENST00000265104.4:c.3834+21C>T	ENSP00000265104.4:n.3834+21C>T
NM_001369.2:c.3834+21C>T	NP_001360.1:n.3834+21C>T
XM_005248262.2:c.3789+21C>T	XP_005248319.1:n.3789+21C>T
XM_011513990.1:c.3834+21C>T	XP_011512292.1:n.3834+21C>T
XR_925598.1:n.4041+21C>T
XM_005248262.3:c.3942+21C>T	XP_005248319.2:n.3942+21C>T
XM_017009177.1:c.3942+21C>T	XP_016864666.1:n.3942+21C>T
XM_017009178.1:c.2847+21C>T	XP_016864667.1:n.2847+21C>T
XM_017009179.2:c.2847+21C>T	XP_016864668.1:n.2847+21C>T
XM_017009180.1:c.3942+21C>T	XP_016864669.1:n.3942+21C>T
XM_017009181.1:c.3942+21C>T	XP_016864670.1:n.3942+21C>T
XM_017009182.1:c.3942+21C>T	XP_016864671.1:n.3942+21C>T
XM_017009183.1:c.3942+21C>T	XP_016864672.1:n.3942+21C>T
XM_017009184.1:c.3942+21C>T	XP_016864673.1:n.3942+21C>T
XM_017009187.1:c.3942+21C>T	XP_016864676.1:n.3942+21C>T
XM_024454388.1:c.2847+21C>T	XP_024310156.1:n.2847+21C>T
XM_024454389.1:c.2436+21C>T	XP_024310157.1:n.2436+21C>T
XR_001742034.1:n.3959+21C>T
XR_001742035.1:n.3959+21C>T
NM_001369.3:c.3834+21C>T MANE Select	NP_001360.1:n.3834+21C>T