Canonical Allele Identifier: CA359188733

Gene: DNAH5

Linked Data

• gnomAD v4: 5-13692108-C-T
• MyVariant Identifiers: chr5:g.13692217C>T (hg19) ; chr5:g.13692108C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.13692108C>T , CM000667.2:g.13692108C>T	GRCh38
NC_000005.9:g.13692217C>T , CM000667.1:g.13692217C>T	GRCh37
NC_000005.8:g.13745217C>T	NCBI36
NG_013081.1:g.257373G>A
NG_013081.2:g.257373G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683611.1:n.1084G>A
ENST00000265104.5:c.13751G>A MANE Select	ENSP00000265104.4:p.Cys4584Tyr
ENST00000681290.1:c.13706G>A	ENSP00000505288.1:p.Cys4569Tyr
ENST00000265104.4:c.13751G>A	ENSP00000265104.4:p.Cys4584Tyr
NM_001369.2:c.13751G>A	NP_001360.1:p.Cys4584Tyr
XM_005248262.2:c.13706G>A	XP_005248319.1:p.Cys4569Tyr
XM_005248262.3:c.13859G>A	XP_005248319.2:p.Cys4620Tyr
XM_017009177.1:c.13439G>A	XP_016864666.1:p.Cys4480Tyr
XM_017009178.1:c.12764G>A	XP_016864667.1:p.Cys4255Tyr
XM_017009179.2:c.12764G>A	XP_016864668.1:p.Cys4255Tyr
XM_017009185.1:c.8948G>A	XP_016864674.1:p.Cys2983Tyr
XM_017009186.1:c.8501G>A	XP_016864675.1:p.Cys2834Tyr
XM_017009188.1:c.7838G>A	XP_016864677.1:p.Cys2613Tyr
XM_024454388.1:c.12764G>A	XP_024310156.1:p.Cys4255Tyr
XM_024454389.1:c.12353G>A	XP_024310157.1:p.Cys4118Tyr
NM_001369.3:c.13751G>A MANE Select	NP_001360.1:p.Cys4584Tyr