Canonical Allele Identifier: CA359204412

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13770810-T-C
• MyVariant Identifiers: chr5:g.13770919T>C (hg19) ; chr5:g.13770810T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770810T>C , CM000667.2:g.13770810T>C	GRCh38
NC_000005.9:g.13770919T>C , CM000667.1:g.13770919T>C	GRCh37
NC_000005.8:g.13823919T>C	NCBI36
NG_013081.1:g.178671A>G
NG_013081.2:g.178671A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9544A>G MANE Select	ENSP00000265104.4:p.Ile3182Val
ENST00000681290.1:c.9499A>G	ENSP00000505288.1:p.Ile3167Val
ENST00000265104.4:c.9544A>G	ENSP00000265104.4:p.Ile3182Val
ENST00000504001.3:n.256A>G
NM_001369.2:c.9544A>G	NP_001360.1:p.Ile3182Val
XM_005248262.2:c.9499A>G	XP_005248319.1:p.Ile3167Val
XM_005248262.3:c.9652A>G	XP_005248319.2:p.Ile3218Val
XM_017009177.1:c.9652A>G	XP_016864666.1:p.Ile3218Val
XM_017009178.1:c.8557A>G	XP_016864667.1:p.Ile2853Val
XM_017009179.2:c.8557A>G	XP_016864668.1:p.Ile2853Val
XM_017009180.1:c.9652A>G	XP_016864669.1:p.Ile3218Val
XM_017009181.1:c.9652A>G	XP_016864670.1:p.Ile3218Val
XM_017009182.1:c.9652A>G	XP_016864671.1:p.Ile3218Val
XM_017009183.1:c.9652A>G	XP_016864672.1:p.Ile3218Val
XM_017009185.1:c.4741A>G	XP_016864674.1:p.Ile1581Val
XM_017009186.1:c.4294A>G	XP_016864675.1:p.Ile1432Val
XM_017009188.1:c.3631A>G	XP_016864677.1:p.Ile1211Val
XM_024454388.1:c.8557A>G	XP_024310156.1:p.Ile2853Val
XM_024454389.1:c.8146A>G	XP_024310157.1:p.Ile2716Val
NM_001369.3:c.9544A>G MANE Select	NP_001360.1:p.Ile3182Val