Canonical Allele Identifier: CA359202092

Gene: DNAH5

Linked Data

• ClinVar Variation Id: 943165
• ClinVar RCV Id: RCV001213300 ; RCV001580018
• dbSNP Id: rs1752923333
• gnomAD v4: 5-13769079-G-A
• MyVariant Identifiers: chr5:g.13769188G>A (hg19) ; chr5:g.13769079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13769079G>A , CM000667.2:g.13769079G>A	GRCh38
NC_000005.9:g.13769188G>A , CM000667.1:g.13769188G>A	GRCh37
NC_000005.8:g.13822188G>A	NCBI36
NG_013081.1:g.180402C>T
NG_013081.2:g.180402C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9778C>T MANE Select	ENSP00000265104.4:p.Gln3260Ter
ENST00000681290.1:c.9733C>T	ENSP00000505288.1:p.Gln3245Ter
ENST00000265104.4:c.9778C>T	ENSP00000265104.4:p.Gln3260Ter
ENST00000504001.3:n.490C>T
NM_001369.2:c.9778C>T	NP_001360.1:p.Gln3260Ter
XM_005248262.2:c.9733C>T	XP_005248319.1:p.Gln3245Ter
XM_005248262.3:c.9886C>T	XP_005248319.2:p.Gln3296Ter
XM_017009177.1:c.9886C>T	XP_016864666.1:p.Gln3296Ter
XM_017009178.1:c.8791C>T	XP_016864667.1:p.Gln2931Ter
XM_017009179.2:c.8791C>T	XP_016864668.1:p.Gln2931Ter
XM_017009180.1:c.9886C>T	XP_016864669.1:p.Gln3296Ter
XM_017009181.1:c.9886C>T	XP_016864670.1:p.Gln3296Ter
XM_017009182.1:c.9886C>T	XP_016864671.1:p.Gln3296Ter
XM_017009185.1:c.4975C>T	XP_016864674.1:p.Gln1659Ter
XM_017009186.1:c.4528C>T	XP_016864675.1:p.Gln1510Ter
XM_017009188.1:c.3865C>T	XP_016864677.1:p.Gln1289Ter
XM_024454388.1:c.8791C>T	XP_024310156.1:p.Gln2931Ter
XM_024454389.1:c.8380C>T	XP_024310157.1:p.Gln2794Ter
NM_001369.3:c.9778C>T MANE Select	NP_001360.1:p.Gln3260Ter