Canonical Allele Identifier: CA359200014

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13829586-C-A
• MyVariant Identifiers: chr5:g.13829695C>A (hg19) ; chr5:g.13829586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13829586C>A , CM000667.2:g.13829586C>A	GRCh38
NC_000005.9:g.13829695C>A , CM000667.1:g.13829695C>A	GRCh37
NC_000005.8:g.13882695C>A	NCBI36
NG_013081.1:g.119895G>T
NG_013081.2:g.119895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683090.1:n.1299G>T
ENST00000265104.5:c.6368G>T MANE Select	ENSP00000265104.4:p.Gly2123Val
ENST00000681290.1:c.6323G>T	ENSP00000505288.1:p.Gly2108Val
ENST00000265104.4:c.6368G>T	ENSP00000265104.4:p.Gly2123Val
NM_001369.2:c.6368G>T	NP_001360.1:p.Gly2123Val
XM_005248262.2:c.6323G>T	XP_005248319.1:p.Gly2108Val
XM_011513990.1:c.6368G>T	XP_011512292.1:p.Gly2123Val
XR_925598.1:n.6575G>T
XM_005248262.3:c.6476G>T	XP_005248319.2:p.Gly2159Val
XM_017009177.1:c.6476G>T	XP_016864666.1:p.Gly2159Val
XM_017009178.1:c.5381G>T	XP_016864667.1:p.Gly1794Val
XM_017009179.2:c.5381G>T	XP_016864668.1:p.Gly1794Val
XM_017009180.1:c.6476G>T	XP_016864669.1:p.Gly2159Val
XM_017009181.1:c.6476G>T	XP_016864670.1:p.Gly2159Val
XM_017009182.1:c.6476G>T	XP_016864671.1:p.Gly2159Val
XM_017009183.1:c.6476G>T	XP_016864672.1:p.Gly2159Val
XM_017009184.1:c.6476G>T	XP_016864673.1:p.Gly2159Val
XM_017009185.1:c.1565G>T	XP_016864674.1:p.Gly522Val
XM_017009186.1:c.1118G>T	XP_016864675.1:p.Gly373Val
XM_017009187.1:c.6476G>T	XP_016864676.1:p.Gly2159Val
XM_017009188.1:c.455G>T	XP_016864677.1:p.Gly152Val
XM_024454388.1:c.5381G>T	XP_024310156.1:p.Gly1794Val
XM_024454389.1:c.4970G>T	XP_024310157.1:p.Gly1657Val
XR_001742034.1:n.6493G>T
XR_001742035.1:n.6493G>T
NM_001369.3:c.6368G>T MANE Select	NP_001360.1:p.Gly2123Val