Canonical Allele Identifier: CA2673270335

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13752358-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13752358T>C , CM000667.2:g.13752358T>C	GRCh38
NC_000005.9:g.13752467T>C , CM000667.1:g.13752467T>C	GRCh37
NC_000005.8:g.13805467T>C	NCBI36
NG_013081.1:g.197123A>G
NG_013081.2:g.197123A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.10873-69A>G MANE Select	ENSP00000265104.4:n.10873-69A>G
ENST00000681290.1:c.10828-69A>G	ENSP00000505288.1:n.10828-69A>G
ENST00000265104.4:c.10873-69A>G	ENSP00000265104.4:n.10873-69A>G
NM_001369.2:c.10873-69A>G	NP_001360.1:n.10873-69A>G
XM_005248262.2:c.10828-69A>G	XP_005248319.1:n.10828-69A>G
XM_005248262.3:c.10981-69A>G	XP_005248319.2:n.10981-69A>G
XM_017009177.1:c.10981-69A>G	XP_016864666.1:n.10981-69A>G
XM_017009178.1:c.9886-69A>G	XP_016864667.1:n.9886-69A>G
XM_017009179.2:c.9886-69A>G	XP_016864668.1:n.9886-69A>G
XM_017009180.1:c.10981-69A>G	XP_016864669.1:n.10981-69A>G
XM_017009181.1:c.10981-69A>G	XP_016864670.1:n.10981-69A>G
XM_017009182.1:c.10981-69A>G	XP_016864671.1:n.10981-69A>G
XM_017009185.1:c.6070-69A>G	XP_016864674.1:n.6070-69A>G
XM_017009186.1:c.5623-69A>G	XP_016864675.1:n.5623-69A>G
XM_017009188.1:c.4960-69A>G	XP_016864677.1:n.4960-69A>G
XM_024454388.1:c.9886-69A>G	XP_024310156.1:n.9886-69A>G
XM_024454389.1:c.9475-69A>G	XP_024310157.1:n.9475-69A>G
NM_001369.3:c.10873-69A>G MANE Select	NP_001360.1:n.10873-69A>G