Canonical Allele Identifier: CA3202520

Gene: DNAH5

Linked Data

• dbSNP Id: rs772990787
• ExAC: 5:13770912 C / A
• gnomAD v3: 5-13770803-C-A
• gnomAD v4: 5-13770803-C-A
• MyVariant Identifiers: chr5:g.13770912C>A (hg19) ; chr5:g.13770803C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13770803C>A , CM000667.2:g.13770803C>A	GRCh38
NC_000005.9:g.13770912C>A , CM000667.1:g.13770912C>A	GRCh37
NC_000005.8:g.13823912C>A	NCBI36
NG_013081.1:g.178678G>T
NG_013081.2:g.178678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265104.5:c.9551G>T MANE Select	ENSP00000265104.4:p.Gly3184Val
ENST00000681290.1:c.9506G>T	ENSP00000505288.1:p.Gly3169Val
ENST00000265104.4:c.9551G>T	ENSP00000265104.4:p.Gly3184Val
ENST00000504001.3:n.263G>T
NM_001369.2:c.9551G>T	NP_001360.1:p.Gly3184Val
XM_005248262.2:c.9506G>T	XP_005248319.1:p.Gly3169Val
XM_005248262.3:c.9659G>T	XP_005248319.2:p.Gly3220Val
XM_017009177.1:c.9659G>T	XP_016864666.1:p.Gly3220Val
XM_017009178.1:c.8564G>T	XP_016864667.1:p.Gly2855Val
XM_017009179.2:c.8564G>T	XP_016864668.1:p.Gly2855Val
XM_017009180.1:c.9659G>T	XP_016864669.1:p.Gly3220Val
XM_017009181.1:c.9659G>T	XP_016864670.1:p.Gly3220Val
XM_017009182.1:c.9659G>T	XP_016864671.1:p.Gly3220Val
XM_017009183.1:c.9659G>T	XP_016864672.1:p.Gly3220Val
XM_017009185.1:c.4748G>T	XP_016864674.1:p.Gly1583Val
XM_017009186.1:c.4301G>T	XP_016864675.1:p.Gly1434Val
XM_017009188.1:c.3638G>T	XP_016864677.1:p.Gly1213Val
XM_024454388.1:c.8564G>T	XP_024310156.1:p.Gly2855Val
XM_024454389.1:c.8153G>T	XP_024310157.1:p.Gly2718Val
NM_001369.3:c.9551G>T MANE Select	NP_001360.1:p.Gly3184Val